Terrestrial Animal Health Code

Contents | Index Chapter 1.9. SECTION 1. Chapter 1.11.

Chapter 1.10.


Application for official recognition by the OIE of free status for contagious bovine pleuropneumonia


Article 1.10.1.


Country free from infection with Mycoplasma mycoides subsp. mycoides SC (contagious bovine pleuropneumonia)

The following information should be provided by OIE Member Countries to support applications for official recognition of status as a country free from infection with Mycoplasma mycoides subsp. mycoides SC (MMmsSC) in accordance with Chapter 11.5. of the Terrestrial Code.

The dossier provided to the OIE should address concisely all the following topics under the headings provided to describe the actual situation in the country and the procedures currently applied, explaining how these comply with the Terrestrial Code.

The terminology defined in the OIE Terrestrial Code and Terrestrial Manual should be referred to and used in compiling the dossier.

National legislation, regulations and Veterinary Authority directives may be referred to and annexed as appropriate in one of the OIE official languages. Weblinks to supporting documents in one of the official languages of the OIE may also be provided, where they exist.

All annexes should be provided in one of the OIE official languages.

The Delegate of the Member Country applying for recognition of CBPP freedom for a country must demonstrate compliance with the Terrestrial Code. That is, the Delegate should submit documentary evidence that the provisions of Article 11.5.3. have been properly implemented and supervised.

In addition, the Delegate of the Member Country must submit a declaration indicating that:

  1. there has been no case of infection with MMmsSC during the past 24 months;

  2. no evidence of infection with MMmsSC has been found during the past 24 months;

  3. no vaccination against CBPP has been carried out during the past 24 months.

In addition, the Delegate of the Member Country applying for recognition of historical freedom must also submit documentary evidence that the provisions of point 1 a) of Article 1.4.6. of the Terrestrial Code have been properly implemented and supervised.

  1. Introduction

    1. Geographical features (rivers, mountain ranges, etc.). Provide a general description of the country and, where relevant, of the region, including physical, geographical and other factors that are relevant to introduction of infection and spread of MMmsSC, taking into account the countries sharing common borders and other epidemiologic pathways for the potential introduction of infection. Provide maps identifying the features above. Specify whether the application includes any noncontiguous territories.

    2. Livestock demographics. Describe the composition of the livestock industry in the country. In particular, describe:

      1. the susceptible animal population by species and types of production systems;

      2. the number of herds, etc. of each susceptible species;

      3. their geographical distribution;

      4. herd density;

      5. the degree of integration and role of producer organisations in the different production systems;

      6. any recent significant changes observed in the production (attach relevant documents if available).

      Provide tables and maps.

    3. Wildlife demographics. What susceptible captive wild, wild or feral species are present in the country? Provide estimates of population sizes and geographic distribution. What are the measures in place to prevent contact between domestic and susceptible wildlife species?

    4. Slaughterhouses/abattoirs, markets and events associated with the congregation of susceptible livestock (e.g. fairs, shows, competitions). What are the major livestock marketing or collection centres? What are the patterns of movement of domestic susceptible species for marketing within the country? How are the susceptible animals sourced, transported and handled during these transactions? Provide maps as appropriate.

  2. Veterinary system

    1. Legislation. Provide a table (and when available a weblink) listing all relevant veterinary legislation, regulations and Veterinary Authority directives in relation to CBPP and a brief description of the relevance of each. The table should include, but not be limited to, the legislation on disease control measures and compensation systems.

    2. Veterinary Services. Describe how the Veterinary Services of the country comply with Chapters 1.1., 3.1. and 3.2. of the Terrestrial Code. Describe how the Veterinary Services supervise, control, enforce and monitor all CBPP-related activities. Provide maps, figures and tables wherever possible.

    3. Provide information on any OIE PVS evaluation conducted in the country and follow-up steps within the PVS Pathway and highlight the results relevant to CBPP and the susceptible species.

    4. Provide a description of the involvement and the participation of industry, producers, farmers, including subsistence and small-scale producers, keepers, veterinary paraprofessionals including community animal health workers, and other relevant groups in CBPP surveillance and control. Provide a description of the role and structure of the private veterinary sector, including number of veterinarians and their distribution, in CBPP surveillance and control. Include a description of continuing education and awareness programmes on CBPP at all relevant levels.

    5. Animal identification, registration, traceability and movement control. Are susceptible animals identified (individually or at a group level)? Provide a description of the traceability system, including methods of animal identification and establishmentor herd registration, applicable to all susceptible species. How are animal movements controlled in the country for all susceptible species? Provide evidence of the effectiveness of animal identification and movement controls and a table describing the number, species, origin and destination of the animals and their products moved within the country in the past 24 months. Provide information on pastoralism, transhumance and related paths of movement.

      Describe the risk management strategy for uncontrolled movements of susceptible species (e.g. seasonal migration).

      Describe the actions available under national legislation. Provide information on illegal movements detected in the past 24 months and the action taken.

  3. CBPP eradication

    1. History. If infection has never occurred in the country, or has not occurred within the past 25 years, state explicitly whether or not the country is applying for recognition of historical freedom according to point 1 a) Article 1.4.6. of the Terrestrial Code.

      If infection has occurred in the country within the past 25 years, provide a description of the CBPP history in the country, with emphasis on recent years. If applicable, provide tables and maps showing the date of first detection, the sources and routes of introduction of infection, the temporal and spatial distribution (number and location of outbreaks per year), the susceptible species involved, and the date of last case or eradication in the country.

    2. Strategy. Describe how CBPP was controlled and eradicated (e.g. slaughter policy, zoning, vaccination, movement control). Provide the time frame for eradication. Describe and justify the corrective actions that have been implemented to prevent future outbreaks of CBPP in response to any past incursions of MMmsSC.

    3. Vaccines and vaccination. Briefly answer the following:

      1. Is there any legislation that prohibits vaccination? If so:

        • Provide the date when vaccination was formally prohibited;

        • Provide information on cases of detection of illegal vaccination during the reporting period and actions taken in response to the detection.

      2. Was vaccination ever used in the country? If so:

        • Provide the date when the last vaccination was carried out;

        • What type of vaccine was used?

        • What species were vaccinated?

        • How were vaccinated animals identified?

        • What was the fate of those animals?

      3. In addition, if vaccination was applied during the past 24 months, provide a description and justification of the vaccination strategy and programme, including the following:

        • the vaccine strains;

        • the species vaccinated;

        • identification of vaccinated animals;

        • the way in which the vaccination of animals was certified or reported and the records maintained;

        • evidence that the vaccine used complies with Chapter 2.4.8. of the Terrestrial Manual.

    4. Provide a description of the legislation, organisation and implementation of the eradication campaign. Outline the legislation applicable to the eradication and how the campaign was organised at different levels. Indicate if detailed operational guidelines exist and give a brief summary.

  4. CBPP diagnosis

    Provide documentary evidence that the relevant provisions of Chapters 1.1.2., 1.1.3. and 2.4.8. of the Terrestrial Manual are applied. The following points should be addressed:

    1. Is CBPP laboratory diagnosis carried out in the country? If so, provide an overview of the CBPP-approved laboratories in the country, including the following:

      1. How the work is shared between different laboratories, logistics for shipment of samples, the follow-up procedures and the time frame for reporting results;

      2. Details of test capability and the types of tests undertaken, including procedures to isolate and identify M. mycoides subsp. mycoides(Mmm), and their performance for their applied use (specificity and sensitivity per type of test). Provide details of the number of CBPP tests performed in the past 24 months in national laboratories and in laboratories in other countries, if relevant;

      3. Procedures for quality assurance and for the official accreditation of laboratories. Give details of formal internal quality management systems, e.g. Good Laboratory Practice, ISO, etc. that exist in, or are planned for, the laboratory system;

      4. Provide details of performance in inter-laboratory validation tests (ring trials), including the most recent results and, if applicable, the corrective measures applied;

      5. Provide details of the handling of live pathogenic agent, including a description of the biosecurity and biosafety measures applied;

      6. Provide a table identifying the tests carried out by each of the laboratories where they are performed, the quality accreditation and biosecurity standards followed and the proficiency tests carried out.

    2. If CBPP laboratory diagnosis is not carried out in the country, provide the names of the laboratories in other countries providing the service as well as the arrangements in place, including logistics for shipment of samples and the time frame for reporting results.

  5. CBPP surveillance

    Provide documentary evidence that surveillance for CBPP in the country complies with Articles 11.5.13. to 11.5.17. of the Terrestrial Code and Chapter 2.4.8. of the Terrestrial Manual. The following information should be included :

    1. What are the criteria for raising a suspicion of CBPP? What is the procedure to notify (by whom and to whom) and what incentives are there for reporting and what penalties are involved for failure to report?

    2. Describe how clinical surveillance is conducted, including which sectors of the livestock production system are included in clinical surveillance, such as establishments, markets, fairs, slaughterhouses/abattoirs, check points, etc.

      Provide a summary table indicating, for the past 24 months, the number of suspected cases, the number of samples tested for CBPP, species, type of sample, testing methods and results (including differential diagnosis). Provide an indication of the timelines of the response including completion of testing to confirm or exclude CBPP. Provide details of follow-up actions taken on all suspicious and positive results.

    3. Serological surveillance. Explain whether serological surveys are conducted and, if so, how frequently and for what purpose. Provide detailed information on the target population, design prevalence, confidence level, sample size, stratification, sampling methods and diagnostic tests used in accordance with Articles 11.5.13. to 11.5.17. of the Terrestrial Code.

    4. Slaughterhouses/abattoirs and slaughter slabs. What are the criteria for raising a suspicion of CBPP lesion? What is the procedure to notify (by whom and to whom)? Provide a summary table indicating, for the past 24 months, the number of suspected cases, the number of samples tested for CBPP agent, species, type of sample, testing methods and results (including differential diagnosis).

    5. For countries where a significant proportion of animals are not slaughtered in controlled slaughterhouses/abattoirs, what are the alternative surveillance measures applied to detect CBPP (e.g. active clinical surveillance programmes, laboratory follow-up).

    6. Provide a description of the means employed during the 24 months preceding this application to rule out the presence of CBPP in the susceptible population. Provide criteria for selection of populations for targeted surveillance and numbers of animals examined and samples tested. Provide details of the methods selected and applied for monitoring the performance of the surveillance programme including indicators.

    7. Provide details of the oversight of surveillance programmes by the Veterinary Services including training programmes for personnel involved in clinical and slaughterhouse/abattoirsurveillance, and the approaches used to increase community involvement in CBPP surveillance programmes.

  6. CBPP prevention

    Describe the procedures in place to prevent the introduction of CBPP into the country, including details of:

    1. Coordination with other countries. Describe any relevant factors in neighbouring countries that should be taken into account (e.g. size, distance from the border to affected herds or animals). Describe coordination, collaboration and information-sharing activities with other countries in the same region or ecosystem.

      Are protection zones in place? If so, provide details of the measures that are applied (e.g. vaccination, intensified surveillance, density control of susceptible species), and provide a geo-referenced map of the zones.

    2. Describe the measures implemented to effectively prevent the introduction of the pathogenic agent, taking into consideration physical or geographical barriers. Describe the measures implemented to prevent the spread of the pathogenic agent within the country. Provide evidence that measures to reduce transmission of CBPP are in place at markets, such as enhancing awareness of CBPP transmission mechanisms and human behaviour that can interrupt transmission, and implementation of good biosecurity, hygiene and disinfection routines at critical points all along the production and marketing networks (typically where animals are being moved and marketed through the country or region).

    3. Import control procedures

      Provide information on countries, zones or compartments from which the country authorises the import of susceptible animals or their products into the country. Describe the criteria applied to approve such countries, zones or compartments, the controls applied to entry of such animals and products, and subsequent internal movement. Describe the import measures (e.g. quarantine) and test procedures required. Advise whether imported animals of susceptible species are required to undergo a quarantine or isolation period and, if so, the duration and location of quarantine. Advise whether import permits and international veterinary certificates are required.

      Describe any other procedures used for assessing the risks posed by import of susceptible animals or their products. Provide summary statistics on imports of susceptible animals and their products for at least the past 24 months, including temporary import and re-entry, specifying countries, zones or compartments of origin, species and the quantity or volume and eventual destination in the country.

      Provide information on whether or not outbreaks have been related to imports or transboundary movements of domestic animals.

      1. Provide a map showing the number and location of all ports, airports and land border crossings. Describe the management structure, staffing levels and resources of the service responsible for import controls and its accountability to the central Veterinary Services. Describe the communication systems between the central authorities and the border posts, and between border posts.

      2. Cite the regulations and describe procedures, type and frequency of checks, and management of noncompliance at the points of entry into the country or their final destination, concerning the import and follow-up of the following:

        • animals;

        • genetic material (semen, oocytes and embryos);

        • Mmm strains including vaccines;

        • veterinary medicinal products;

        • other materials at risk of being contaminated with Mmm.

  7. Control measures and contingency planning

    1. List any written guidelines, including contingency plans, available to the Veterinary Services for dealing with suspected or confirmed outbreaks of CBPP. The contingency plan should be attached as an annex in one of the OIE official languages. If not available, provide a brief summary of what is covered. Provide information on any simulation exercise for CBPP that was conducted in the country in the past five years.

    2. In the event of a suspected or confirmed CBPP outbreak:

      1. Are quarantine measures imposed on establishments with suspected cases, pending final diagnosis? What other procedures are followed with respect to suspected cases (e.g. livestock standstills)?

      2. Indicate the sampling, dispatch and testing procedures that would be used to identify and confirm presence of the pathogenic agent;

      3. Describe the actions that would be taken to control the disease situation in and around the establishments where the outbreak is confirmed;

      4. Provide a detailed description of the control or eradication procedures (e.g. forward and backward tracing, disinfection of establishments, vehicles and equipment, including verification methods, vaccination, stamping-out policy, slaughter policy, movement control, pastured livestock and livestock as pets, control of offal, especially lungs, and carcasses, methods of disposal of carcasses and other contaminated products or materials, decontamination, campaigns to promote awareness of farmers) that would be taken. In the case of emergency vaccination, indicate the source and type of vaccine and provide details of any vaccine supply scheme and stocks;

      5. Describe the criteria and procedures that would be used to confirm that an outbreak has been successfully controlled or eradicated, including restocking strategies, use of sentinel animals, serological surveillance programmes, etc.;

      6. Give details of any compensation that would be made available to owners, farmers, etc. when animals are slaughtered for disease control or eradication purposes and the prescribed timetable for payments;

      7. Describe how control efforts, including vaccination and biosecurity, would target critical risk control points.

  8. Recovery of free status

    Member Countries applying for recognition of recovery of free status for a country should comply with the provisions of Article 11.5.4. of the Terrestrial Code and provide detailed information as specified in Sections 3 a), 3 b), 3 c), 5 a), 5 b), 5 c) and 5 d) of this questionnaire. Information in relation to other sections need only be supplied if relevant.


Article 1.10.2.


Zone free from infection with Mycoplasma mycoides subsp. mycoides SC (contagious bovine pleuropneumonia)

The following information should be provided by OIE Member Countries to support applications for official recognition of status as a zone free from infection with Mycoplasma mycoides subsp. mycoides SC (MMmsSC) in accordance with Chapter 11.5. of the Terrestrial Code.

The dossier provided to the OIE should address concisely all the following topics under the headings provided to describe the actual situation in the country and the procedures currently applied, explaining how these comply with the Terrestrial Code.

The terminology defined in the OIE Terrestrial Code and Terrestrial Manual should be referred to and used in compiling the dossier.

National legislation, regulations and Veterinary Authority directives may be referred to and annexed as appropriate in one of the OIE official languages. Weblinks to supporting documents in one of the official languages of the OIE may also be provided, where they exist.

All annexes should be provided in one of the OIE official languages.

The Delegate of the Member Country applying for recognition of CBPP freedom for a zone must demonstrate compliance with the Terrestrial Code. That is, the Delegate should submit documentary evidence that the provisions of Article 11.5.3. have been properly implemented and supervised.

In addition, the Delegate of the Member Country must submit a declaration indicating that:

  1. there has been no case of infection with MMmsSC during the past 24 months;

  2. no evidence of infection with MMmsSC has been found during the past 24 months;

  3. no vaccination against CBPP has been carried out during the past 24 months.

In addition, the Delegate of the Member Country applying for recognition of historical freedom must also submit documentary evidence that the provisions of point 1 a) of Article 1.4.6. of the Terrestrial Code have been properly implemented and supervised.

  1. Introduction

    1. Geographical features (rivers, mountain ranges, etc.). Provide a general description of the country and the zone, and where relevant of the region, including physical, geographical and other factors that are relevant to introduction of infection and spread of MMmsSC, taking into account the countries or zones sharing common borders and other epidemiologic pathways for the potential introduction of infection.

      The boundaries of the zone must be clearly defined, including a protection zone if applied. Provide maps identifying the features above, including a digitalised, geo-referenced map with a precise text description of the geographical boundaries of the zone.

    2. Livestock demographics. Describe the composition of the livestock industry in the country and the zone. In particular, describe:

      1. the susceptible animal population by species and types of production systems in the country and the zone;

      2. the number of herds, etc. of each susceptible species;

      3. their geographical distribution;

      4. herd density;

      5. the degree of integration and role of producer organisations in the different production systems;

      6. any recent significant changes observed in the production (attach relevant documents if available).

      Provide tables and maps.

    3. Wildlife demographics. What susceptible captive wild, wild or feral species are present in the country and the zone? Provide estimates of population sizes and geographic distribution. What are the measures in place to prevent contact between domestic and susceptible wildlife species?

    4. Slaughterhouses/abattoirs, markets and events associated with the congregation of susceptible livestock (e.g. fairs, shows, competitions). Where are the major livestock marketing or collection centres? What are the patterns of movement of domestic susceptible species for marketing within the country or zone, and between zones of the same or different status? How are the susceptible animals sourced, transported and handled during these transactions? Provide maps as appropriate.

  2. Veterinary system

    1. Legislation. Provide a table (and when available a weblink) listing all relevant veterinary legislation, regulations and Veterinary Authority directives in relation to CBPP and a brief description of the relevance of each. The table should include, but not be limited to, the legislation on disease control measures and compensation systems.

    2. Veterinary Services. Describe how the Veterinary Services of the country comply with Chapters 1.1., 3.1. and 3.2. of the Terrestrial Code. Describe how the Veterinary Services supervise, control, enforce and monitor all CBPP-related activities. Provide maps, figures and tables wherever possible.

    3. Provide information on any OIE PVS evaluation conducted in the country and follow-up steps within the PVS Pathway and highlight the results relevant to CBPP and the susceptible species.

    4. Provide a description of the involvement and the participation of industry, producers, farmers, including subsistence and small-scale producers, keepers, veterinary paraprofessionals including community animal health workers, and other relevant groups in CBPP surveillance and control. Provide a description of the role and structure of the private veterinary sector, including the number of veterinarians and their distribution, in CBPP surveillance and control. Include a description of continuing education and awareness programmes on CBPP at all relevant levels.

    5. Animal identification, registration, traceability and movement control. Are susceptible animals identified (individually or at a group level)? Provide a description of the traceability system, including methods of animal identification and establishment or herd registration, applicable to all susceptible species. How are animal movements controlled in and between zones of the same or different status for all susceptible species? Provide evidence of the effectiveness of animal identification and movement controls and a table describing the number, species, origin and destination of the animals and their products moved within the country in the past 24 months. Provide information on pastoralism, transhumance and related paths of movement.

      Describe the risk management strategy for uncontrolled movements of susceptible species (e.g. seasonal migration).

      Describe the actions available under national legislation. Provide information on illegal movements detected in the past 24 months and the action taken.

  3. CBPP eradication

    1. History. If infection has never occurred in the zone, or has not occurred within the past 25 years, state explicitly whether or not the zone is applying for recognition of historical freedom in the zone according to point 1 a) of Article 1.4.6. of the Terrestrial Code.

      If infection has occurred in the zone within the past 25 years, provide a description of the CBPP history in the country and zone, with emphasis on recent years. If applicable, provide tables and maps showing the date of first detection, the sources and routes of introduction of infection, the temporal and spatial distribution (number and location of outbreaks per year), the susceptible species involved, and the date of last case or eradication in the zone.

    2. Strategy. Describe how CBPP was controlled and eradicated in the zone (e.g. slaughter policy, zoning, vaccination, movement control). Provide the time frame for eradication. Describe and justify the corrective actions that have been implemented to prevent future outbreaks of CBPP in response to any past incursions of MMmsSC.

    3. Vaccines and vaccination. Briefly answer the following:

      1. Is there any legislation that prohibits vaccination? If so:

        • Provide the date when vaccination was formally prohibited;

        • Provide information on cases of detection of illegal vaccination during the reporting period and actions taken in response to the detection.

      2. Was vaccination ever used in the country? If so:

        • Provide the date when the last vaccination was carried out;

        • What type of vaccine was used in the zone and the rest of the country?

        • What species were vaccinated?

        • How were vaccinated animals identified?

        • What was the fate of those animals?

      3. In addition, if vaccination was applied during the past 24 months, provide a description and justification of the vaccination strategy and programme, including the following:

        • the vaccine strains;

        • the species vaccinated;

        • identification of vaccinated animals;

        • the way in which the vaccination of animals was certified or reported and the records maintained;

        • evidence that the vaccine used complies with Chapter 2.4.8. of the Terrestrial Manual.

    4. Provide a description of the legislation, organisation and implementation of the eradication campaign. Outline the legislation applicable to the eradication and how the campaign was organised at different levels. Indicate if detailed operational guidelines exist and give a brief summary.

  4. CBPP diagnosis

    Provide documentary evidence that the relevant provisions of Chapters 1.1.2., 1.1.3. and 2.4.8. of the Terrestrial Manual are applied. The following points should be addressed:

    1. Is CBPP laboratory diagnosis carried out in the country? If so, provide an overview of the CBPP-approved laboratories in the country. Indicate the laboratories where samples originating from the zone are diagnosed. Address the following points:

      1. How the work is shared between different laboratories, logistics for shipment of samples, the follow-up procedures and the time frame for reporting results;

      2. Details of test capability and the types of tests undertaken, including procedures to isolate and identify M. mycoides subsp. mycoides(Mmm), and their performance for their applied use (specificity and sensitivity per type of test). Provide details of the number of CBPP tests performed in the past 24 months in national laboratories and in laboratories in other countries, if relevant;

      3. Procedures for quality assurance and for the official accreditation of laboratories. Give details of formal internal quality management systems, e.g. Good Laboratory Practice, ISO, etc. that exist in, or are planned for, the laboratory system;

      4. Provide details of performance in inter-laboratory validation tests (ring trials), including the most recent results and, if applicable, the corrective measures applied;

      5. Provide details of the handling of live pathogenic agent, including a description of the biosecurity and biosafety measures applied;

      6. Provide a table identifying the tests carried out by each of the laboratories where they are performed, the quality accreditation and biosecurity standards followed and the proficiency tests carried out.

    2. If CBPP laboratory diagnosis is not carried out in the country, provide the names of the laboratories in other countries providing the service as well as the arrangements in place, including logistics for shipment of samples and the time frame for reporting results.

  5. CBPP surveillance

    Provide documentary evidence that surveillance for CBPP in the zone complies with Articles 11.5.13. to 11.5.17. of the Terrestrial Code, and Chapter 2.4.8. of the Terrestrial Manual. The following information should be included:

    1. What are the criteria for raising a suspicion of CBPP? What is the procedure to notify (by whom and to whom) and what incentives are there for reporting and what penalties are involved for failure to report?

    2. Describe how clinical surveillance is conducted, including which sectors of the livestock production system are included in clinical surveillance, such as establishments, markets, fairs, slaughterhouses/abattoirs, check points, etc.

      Provide a summary table indicating, for the past 24 months, the number of suspected cases, the number of samples tested for CBPP, species, type of sample, testing methods and results (including differential diagnosis). Provide an indication of the timelines of the response including completion of testing to confirm or exclude CBPP. Provide details of follow-up actions taken on all suspicious and positive results.

    3. Serological surveillance. Explain whether serological surveys are conducted and, if so, how frequently and for what purpose. Provide detailed information on the target population, design prevalence, confidence level, sample size, stratification, sampling methods and diagnostic tests used in accordance with Articles 11.5.13. to 11.5.17. of the Terrestrial Code.

    4. Slaughterhouses/abattoirs and slaughter slabs. What are the criteria for raising a suspicion of CBPP lesion? What is the procedure to notify (by whom and to whom)? Provide a summary table indicating, for the past 24 months, the number of suspected cases, the number of samples tested for CBPP agent, species, type of sample, testing methods and results (including differential diagnosis).

    5. For countries where a significant proportion of animals in the zone are not slaughtered in controlled slaughterhouses/abattoirs, what are the alternative surveillance measures applied to detect CBPP (e.g. active clinical surveillance programmes, laboratory follow-up).

    6. Provide a description of the means employed during the 24 months preceding this application to rule out the presence of CBPP in the susceptible population of the zone. Provide criteria for selection of populations for targeted surveillance and numbers of animals examined and samples tested in diagnostic laboratories. Provide details of the methods selected and applied for monitoring the performance of the surveillance programme including indicators.

    7. Provide details of the oversight of surveillance programmes by the Veterinary Services including training programmes for personnel involved in clinical and slaughterhouse/abattoirsurveillance, and the approaches used to increase community involvement in CBPP surveillance programmes.

  6. CBPP prevention

    Describe the procedures in place to prevent the introduction of CBPP into the country or zone, including details of:

    1. Coordination with other countries. Describe any relevant factors in neighbouring countries and zones that should be taken into account (e.g. size, distance from the border to affected herds or animals). Describe coordination, collaboration and information-sharing activities with other countries and zones in the same region or ecosystem.

      If the CBPP free zone is established in a CBPP infected country or borders an infected country or zone, describe the animal health measures implemented to effectively prevent the introduction of the pathogenic agent, taking into consideration existing physical or geographical barriers.

      Are protection zones in place? If so, indicate whether or not the protection zones are included in the proposed free zones. Provide details of the measures that are applied (e.g. vaccination, intensified surveillance, density control of susceptible species), and provide a geo-referenced map of the zones.

    2. Describe the measures implemented to effectively prevent the introduction of the pathogenic agent, taking into consideration physical or geographical barriers. Describe the measures implemented to prevent the spread of the pathogenic agent within the country or zone. Provide evidence that measures to reduce transmission of CBPP are in place at markets, such as enhancing awareness of CBPP transmission mechanisms and human behaviour that can interrupt transmission, and implementation of good biosecurity, hygiene and disinfection routines at critical points all along the production and marketing networks (typically where animals are being moved and marketed through the country or region).

    3. Import control procedures

      Provide information on countries, zones or compartments from which the country authorises the import of susceptible animals or their products into the country or zone? Describe the criteria applied to approve such countries, zones or compartments, the controls applied to entry of such animals and products, and subsequent internal movement. Describe the import measures (e.g. quarantine) and test procedures required. Advise whether imported animals of susceptible species are required to undergo a quarantine or isolation period and, if so, the duration and location of quarantine. Advise whether import permits and international veterinary certificates are required.

      Describe any other procedures used for assessing the risks posed by import of susceptible animals or their products. Provide summary statistics on imports of susceptible animals and their products for at least the past 24 months, including temporary import and re-entry, specifying countries, zones or compartments of origin, species and the quantity or volume and eventual destination in the country.

      Provide information on whether or not outbreaks have been related to imports or transboundary movements of domestic animals.

      1. Provide a map showing the number and location of all ports, airports and land border crossings. Describe the management structure, staffing levels and resources of the service responsible for import controls and its accountability to the central Veterinary Services. Describe the communication systems between the central authorities and the border posts, and between border posts.

      2. Cite the regulations and describe procedures, type and frequency of checks, and management of noncompliance at the points of entry into the zone or their final destination, concerning the import and follow-up of the following:

        • animals;

        • genetic material (semen, oocytes and embryos);

        • Mmm strains including vaccines;

        • veterinary medicinal products;

        • other materials at risk of being contaminated with Mmm.

  7. Control measures and contingency planning

    1. List any written guidelines, including contingency plans, available to the Veterinary Services for dealing with suspected or confirmed outbreaks of CBPP. The contingency plan should be attached as an annex in one of the OIE official languages. If not available, provide a brief summary of what is covered . Provide information on any simulation exercise for CBPP that was conducted in the country in the past five years.

    2. In the event of a suspected or confirmed CBPP outbreak:

      1. Are quarantine measures imposed on establishments with suspected cases, pending final diagnosis? What other procedures are followed with respect to suspected cases (e.g. livestock standstills)?

      2. Indicate the sampling, dispatch and testing procedures that would be used to identify and confirm presence of the pathogenic agent;

      3. Describe the actions that would be taken to control the disease situation in and around the establishments where the outbreak is confirmed;

      4. Provide a detailed description of the control or eradication procedures (e.g. forward and backward tracing, disinfection of establishments, vehicles and equipment, including verification methods, vaccination, stamping-out policy, slaughter policy, movement control, pastured livestock and livestock as pets, control of offal, especially lungs, and carcasses, methods of disposal of carcasses and other contaminated products or materials, decontamination, campaigns to promote awareness of farmers) that would be taken. In the case of emergency vaccination, indicate the source and type of vaccine and provide details of any vaccine supply scheme and stocks;

      5. Describe the criteria and procedures that would be used to confirm that an outbreak has been successfully controlled or eradicated, including restocking strategies, use of sentinel animals, serological surveillance programmes, etc.;

      6. Give details of any compensation that would be made available to owners, farmers, etc. when animals are slaughtered for disease control or eradication purposes and the prescribed timetable for payment;

      7. Describe how control efforts, including vaccination and biosecurity, would target critical risk control points.

  8. Recovery of free status

    Member Countries applying for recognition of recovery of free status for a zone should comply with the provisions of Article 11.5.4. of the Terrestrial Code and provide detailed information as specified in Sections 3 a), 3 b), 3 c), 5 a), 5 b), 5 c) and 5 d) of this questionnaire. Information in relation to other sections need only be supplied if relevant.


Article 1.10.3.


Application for endorsement by the OIE of an official control programme for contagious bovine pleuropneumonia

The following information should be provided by OIE Member Countries to support applications for endorsement by the OIE of an official control programme for contagious bovine pleuropneumonia (CBPP) in accordance with Chapter 11.5. of the Terrestrial Code.

The dossier provided to the OIE should address concisely all the following topics under the headings provided in Sections 1 to 4 to describe the actual situation in the country and the procedures currently applied, explaining how these comply with the Terrestrial Code.

In Sections 3 f) o 3 i) describe concisely the work plan and timelines of the control programme for the next five years.

The terminology defined in the OIE Terrestrial Code and Terrestrial Manual should be referred to and used in compiling the dossier.

National legislation, regulations and Veterinary Authority directives may be referred to and annexed as appropriate in one of the OIE official languages. Weblinks to supporting documents in one of the official languages of the OIE may also be provided, where they exist.

All annexes should be provided in one of the OIE official languages.

The Delegate of the Member Country applying for endorsement of the official control programme should submit documentary evidence that the provisions of Article 11.5.18. have been properly implemented and supervised. In addition, the Delegate of the Member Country must submit the detailed national official control programme for CBPP.

  1. Introduction

    1. Geographical features (rivers, mountain ranges, etc.). Provide a general description of the country and zones, and where relevant of the region, including physical, geographical and other factors that are relevant to introduction of infection and spread of MMmsSC, taking into account the countries or zones sharing common borders and other epidemiologic pathways for the potential introduction of infection. Provide maps identifying the features above. Specify whether the application includes any noncontiguous territories.

    2. If the endorsed plan is implemented in stages to specific parts of the country, the boundaries of the zones should be clearly defined, including the protection zones if applied. Provide a digitalised, geo-referenced map with a description of the geographical boundaries of the zones.

    3. Livestock demographics. Describe the composition of the livestock industry in the country and any zones. In particular, describe:

      1. the susceptible animal population by species and types of production systems;

      2. the number of herds, etc. of each susceptible species;

      3. their geographical distribution;

      4. herd density;

      5. the degree of integration and role of producer organisations in the different production systems;

      6. any recent significant changes observed in the production (attach relevant documents if available).

      Provide tables and maps.

    4. Wildlife demographics. What susceptible captive wild, wild or feral species are present in the country and any zones? Provide estimates of population sizes and geographic distribution. What are the measures in place to prevent contact between domestic and susceptible wildlife species?

    5. Slaughterhouses/abattoirs, markets and events associated with the congregation of susceptible livestock (e.g. fairs, shows, competitions). Where are the major livestock marketing or collection centres? What are the patterns of movement of susceptible domestic species for marketing within the country? How are the susceptible animals sourced, transported and handled during these transactions? Provide maps as appropriate.

  2. Veterinary system

    1. Legislation. Provide a table (and when available a weblink) listing all relevant veterinary legislation, regulations and Veterinary Authority directives in relation to the CBPP control programme and a brief description of the relevance of each. The table should include, but not be limited to, the legislation on disease control measures and compensation systems.

    2. Veterinary Services. Describe how the Veterinary Services of the country comply with Chapters 1.1., 3.1. and 3.2. of the Terrestrial Code. Describe how the Veterinary Services supervise, control, enforce and monitor all CBPP-related activities. Provide maps, figures and tables wherever possible.

    3. Provide information on any OIE PVS evaluation conducted in the country and follow-up steps within the PVS Pathway and highlight the results relevant to CBPP and the susceptible species.

    4. Provide a description of the involvement and the participation of industry, producers, farmers, including subsistence and small-scale producers, keepers, veterinary paraprofessionals including community animal health workers, and other relevant groups in CBPP surveillance and control. Provide a description of the role and structure of the private veterinary sector, including the number of veterinarians and their distribution, in CBPP surveillance and control.

      Include a description of continuing education and awareness programmes on CBPP at all relevant levels of the susceptible species value.

    5. Animal identification, registration, traceability and movement control. Are susceptible animals identified (individually or at a group level)? Provide a description of the traceability system, including methods of animal identification and establishment or herd registration, applicable to all susceptible species. How are animal movements controlled in the country for all susceptible species? Provide evidence of the effectiveness of animal identification and movement controls and a table describing the number, species, origin and destination of the animals and their products moved within the country in the past 24 months. Provide information on pastoralism, transhumance and related paths of movement.

      Describe the risk management strategy for uncontrolled movements of susceptible species (e.g. seasonal migration).

      Describe the actions available under national legislation. Provide information on illegal movements detected in the past 24 months and the action taken.

  3. Official control programme for CBPP submitted for OIE endorsement

    Submit a concise plan of the measures for the control and eventual eradication of CBPP in the country, including:

    1. Epidemiology

      1. Describe the CBPP history in the country, with emphasis on recent years. Provide tables and maps showing the date of first detection, the number and location of outbreaks per year, the sources and routes of introduction of infection, the types and subtypes of Mmm present and the date of implementation of the control programme in the country.

      2. Describe the epidemiological situation of CBPP in the country and the surrounding countries or zones highlighting the current knowledge and gaps. Provide maps of:

        • the geography of the country with the relevant information concerning CBPP situation;

        • livestock density and movements and estimated CBPP prevalence.

    2. CBPP surveillance

      Provide documentary evidence that surveillance for CBPP in the country complies with Articles 11.5.14. and 11.5.15. of the Terrestrial Code, and Chapter 2.4.8. of the Terrestrial Manual. The following information should be included:

      1. What are the criteria for raising a suspicion of CBPP? What is the procedure to notify (by whom and to whom) and what incentives are there for reporting and what penalties are involved for failure to report?

      2. Describe how clinical surveillance is conducted, including which sectors of the livestock production system are included in clinical surveillance, such as establishments, markets, fairs, slaughterhouses/abattoirs, check points, etc. Provide details of follow-up actions taken on clinical suspicions.

      3. Serological surveillance. Explain whether serological surveys are conducted and, if so, how frequently and for what purpose. Provide detailed information on the target population, design prevalence, confidence level, sample size, stratification, sampling methods and diagnostic tests used in accordance with Articles 11.5.13. and 11.5.14. of the Terrestrial Code.

      4. Surveillance at slaughterhouses/abattoirs, slaughter slabs. Explain whether slaughterhouse/abattoir surveys are conducted and, if so, how frequently and for what purpose. What are the criteria for suspecting a lesion is CBPP? What is the procedure for notify (by whom and to whom)?

      5. Provide a summary table indicating, for at least the past 24 months, the number of suspected cases, the number of samples tested for CBPP, species, type of sample, testing methods and results (including differential diagnosis). Provide procedural details of follow-up actions taken on suspicious and positive results and on how these findings are interpreted and acted upon.

        Provide criteria for selection of populations for targeted surveillance and numbers of animals examined and samples tested in diagnostic laboratories. Provide details of the methods selected and applied for monitoring the performance of the surveillance programme including indicators.

      6. In countries where a significant proportion of animals in the country or zone are not slaughtered in controlled slaughterhouses/abattoirs, what are the alternative surveillance measures applied to detect CBPP (e.g. active clinical surveillance programme, laboratory follow-up).

      7. Provide information on the level of risk in different husbandry systems, and provide evidence that targeted studies are implemented to address gaps (e.g. targeted serological surveys, active surveillance, participatory epidemiology studies, risk assessments, etc.) and that the acquired knowledge assists in more effective implementation of control measures.

      8. Provide details of the oversight of surveillance programmes by the Veterinary Services including training programmes for personnel involved in clinical and slaughterhouse/abattoirsurveillance, and the approaches used to increase community involvement in CBPP surveillance programmes.

      9. Provide evidence that surveys are carried out to assess vaccination coverage and population immunity of the target populations, show analysis of surveillance data to assess the change in CBPP prevalence over time in the target populations, assess the control measures (cost effectiveness, degree of implementation, impact). Provide information on outcomes of outbreak investigations including outbreaks that have occurred despite control measures, documented inspections showing compliance with biosecurity and hygiene requirements.

    3. CBPP diagnosis

      Provide documentary evidence that the relevant provisions of Chapters 1.1.1., 1.1.3. and 2.4.8. of the Terrestrial Manual are applied. The following points should be addressed:

      1. Is CBPP laboratory diagnosis carried out in the country? If so, provide an overview of the CBPP-approved laboratories in the country, including the following:

        • How the work is shared between different laboratories, logistics for shipment of samples, the follow-up procedures and the time frame for reporting results;

        • Details of test capability and the types of tests undertaken including procedures to isolate and identify M. mycoides subsp. mycoides (Mmm) and their performance for their applied use (specificity and sensitivity per type of test). Provide details of the number of CBPP tests performed in the past 24 months in national laboratories and in laboratories in other countries, if relevant;

        • Procedures for quality assurance and, if available, for the official accreditation of laboratories. Give details of formal internal quality management systems, e.g. Good Laboratory Practice, ISO, etc. that exist in, or are planned for, the laboratory system;

        • Provide details of performance in inter-laboratory validation tests (ring trials), including the most recent results and, if applicable, the corrective measures applied;

        • Provide details of the handling of live pathogenic agent, including a description of the biosecurity and biosafety measures applied;

        • Provide a table identifying the tests carried out by each of the laboratories where they are performed, the quality accreditation and biosecurity standards followed and the proficiency tests carried out.

      2. If CBPP laboratory diagnosis is not carried out in the country, provide the names of the laboratories in other countries providing the service as well as the arrangements in place, including logistics for shipment of samples and the time frame for reporting results.

    4. Strategies

      1. Provide a description of the legislation, organisation and implementation of the current CBPP control programme. Outline the legislation applicable to the control programme and how its implementation is organised at different levels. Indicate if detailed operational guidelines exist and give a brief summary.

      2. Describe CBPP control strategies in the country or any zones, including in terms of animal movement control, fate of infected and in-contact animals, vaccination and possible use of antibiotics. Strategies should be based on the assessment of the CBPP situation in the zones, country and region.

      3. Provide information on what types of vaccines are used and which species are vaccinated. Provide evidence that the vaccine used complies with Chapter 1.1.8. of the Terrestrial Manual. Provide information on the licensing process for the vaccines used. Describe the vaccination programme in the country and in any zones, including records kept, and provide evidence to show its effectiveness, such as vaccination coverage, population immunity, etc. Provide details of the studies carried out to determine the vaccination coverage and the population immunity, including the study designs and the results.

      4. Provide a description of the policy on antibiotic treatment within the strategy. If it is banned how is the ban implemented?

      5. Describe how the stamping-out policy is implemented in the country or any zones and under which circumstances.

      6. In the event of outbreaks, provide evidence of the impact of the control measures already implemented on the reduction in number of outbreaks and their distribution. If possible, provide information on primary and secondary outbreaks.

    5. CBPP prevention

      Describe the procedures in place to prevent the introduction of CBPP into the country, including details of:

      1. Coordination with other countries. Describe any relevant factors in neighbouring countries and zones that should be taken into account (e.g. size, distance from the border to affected herds or animals). Describe coordination, collaboration and information-sharing activities with other countries and zones in the same region or ecosystem.

        Are protection zones in place? If so, provide details of the measures that are applied (e.g. vaccination, intensified surveillance, density control of susceptible species), and provide a geo-referenced map of the zones.

      2. Describe the measures implemented to effectively prevent the introduction of the pathogenic agent, taking into consideration physical or geographical barriers. Describe the measures implemented to prevent the spread of the pathogenic agent within the country or zone. Provide evidence that measures to reduce transmission of CBPP are in place at markets, such as enhancing awareness of CBPP transmission mechanisms and human behaviour that can interrupt transmission, and implementation of good biosecurity, hygiene and disinfection routines at critical points all along the production and marketing networks (typically where animals are being moved and marketed through the country or region).

      3. Import control procedures

        Provide information on countries, zones or compartments from which the country authorises the import of susceptible animals or their products into the country or any zones. Describe the criteria applied to approve such countries, zones or compartments, the controls applied to entry of such animals and products and subsequent internal movement. Describe the import measures (e.g. quarantine) and test procedures required. Advise whether imported animals of susceptible species are required to undergo a quarantine or isolation period and, if so, the duration and location of quarantine. Advise whether import permits and international veterinary certificates are required.

        Describe any other procedures used for assessing the risks posed by import of susceptible animals or their products. Provide summary statistics on imports of susceptible animals and their products for at least the past 24 months, including temporary import and re-entry, specifying countries, zones or compartments of origin, species and the quantity or volume and eventual destination in the country. Provide information on whether or not outbreaks have been related to imports or transboundary movements of domestic animals.

        • Provide a map showing the number and location of all ports, airports and land border crossings. Describe the management structure, staffing levels and resources of the service responsible for import controls and its accountability to the central Veterinary Services. Describe the communication systems between the central authorities and the border posts, and between border posts.

        • Cite the regulations and describe procedures, type and frequency of checks, and management of noncompliance at the points of entry into the country or their final destination, concerning the import and follow-up of the following:

          • animals;

          • genetic material (semen, oocytes and embryos);

          • Mmm strains including vaccines;

          • veterinary medicinal products;

          • other materials at risk of being contaminated with Mmm.

      4. Describe the actions available under national legislation. Provide information on illegal movements detected in the past 24 months and the action taken.

    6. Work plan and timelines of the control programme for the next five years, including cessation of vaccination. Describe the progressive objectives including expected status to be achieved in the next five years: for zones (if applicable) and for the whole country.

    7. Performance indicators and timeline. The performance indicators should relate to the most important areas and steps where improvements in the programme are needed. These may include, but are not restricted to, strengthening Veterinary Services, legislation, clinical and slaughterhouse/abattoir reporting, availability and quality of vaccines, animal identification systems, vaccination coverage, population immunity, movement control, disease awareness, CBPP seroprevalence reduction, cattle owners' participatory perception on the effectiveness of the programme, etc. The progressive reduction of outbreak incidence towards elimination of transmission of Mmm in all susceptible livestock in at least one zone of the country should also be measured and monitored.

    8. Assessment of the evolution of the official control programme since the first date of implementation. This should include documented evidence demonstrating that the control programme has been implemented and that the first results are favourable. Measurable evidence of success such as the performance indicators should include, but not be limited to, vaccination data, decreased prevalence, successfully implemented import measures, control of animal movements and finally decrease or elimination of CBPP outbreaks in the whole country or selected zones as described in the programme. This should include documented evidence of the effective implementation of Sections 3 d) and 3 e) above.

    9. Describe the funding for the control programme and annual budgets for its duration.

  4. Control measures and emergency response

    1. List any written guidelines, including contingency plans, available to the Veterinary Services for dealing with suspected or confirmed outbreaks of CBPP. The contingency plan should be attached as an annex in one of the OIE official languages. If not available, provide a brief summary of what is covered. Provide information on any simulation exercise for CBPP that was conducted in the country in the past five years.

    2. In the event of a suspected or confirmed CBPP outbreak:

      1. Are quarantine measures imposed on establishments with suspected cases, pending final diagnosis? What other procedures are followed regarding suspected cases (e.g. livestock standstills)?

      2. Indicate the sampling, dispatch and testing procedures that would be used to identify and confirm presence of the pathogenic agent;

      3. Describe the actions that would be taken to control the disease situation in and around the establishments where the outbreak is confirmed;

      4. Describe in detail the control or eradication procedures (e.g. forward and backward tracing, disinfection of establishments, vehicles and equipment, including verification methods, vaccination, stamping-out policy, slaughter, movement control, pastured livestock and livestock as pets, control of offal, especially lungs, and carcasses, methods of disposal of carcasses and other contaminated products or materials, decontamination, campaigns to promote awareness of farmers) that would be taken. In the case of emergency vaccination, indicate the source and type of vaccine and provide details of any vaccine supply scheme and stocks;

      5. Describe the criteria and procedures that would be used to confirm that an outbreak has been successfully controlled or eradicated, including restocking strategies, use of sentinel animals, serological surveillance programmes, etc.;

      6. Provide details of any compensation that would be made available to owners, farmers, etc. when animals are slaughtered for disease control or eradication purposes and the prescribed timetable for payments;

      7. Describe how control efforts, including vaccination and biosecurity, would target critical risk control points.


nb: first adopted in 2009; most recent update adopted in 2018.

2018 ©OIE - Terrestrial Animal Health Code

Contents | Index Chapter 1.9. Chapter 1.11.