NBMA Frequently Asked Questions
Biosafety refers to the need to protect human health and the environment from the possible adverse effects of the products of modern biotechnology.
As an Agency of the Federal government, NBMA has the responsibility of regulating modern biotechnology activities and Genetically Modified Organisms in Nigeria. The functions of NBMA include:
- Proposing the overall policy guidance on issues of Biosafety in Nigeria for the approval of the Board;
- Implementing the provisions of the Conventions (Convention on Biological Diversity (CBD)) and the Protocols (Cartagena Protocol on Biosafety, and Kuala Lumpur Protocol on Liability and Redress) on matters relating to GMOs;
- Rendering reports to the Secretariat of the Convention on the implementation of the Convention and Protocol on matters relating to the use of GMOs;
- Developing measures and criteria for risk assessment, peer review and decision making;
- Developing risk management plan and strategy for protecting human health, biological diversity and the environment from potential risks associated with GMOs;
- Accepting, verifying and processing applications in respect of GMOs for Permit and keeping records of all approvals and unapproved applications as contained in Part VIII, subsection 24 (1);
- Taking samples and carrying out laboratory analysis of living materials and products for purposes of determining if they are genetically modified and ensuring compliance with the Act;
- Carrying out actions necessary to ensure compliance with the legal obligations set out in the Act, including, but not limited to, the inspection of facilities undertaking GMO research, conducting research activities with GMOs covered by the Act, the collection and analysis of samples of materials covered by the Act, the monitoring of human health and the environment to determine the effects of GMOs regulated by the Act;
- Liaising with the Secretariat of the Convention and the Biosafety Clearing House (BCH) with respect to the administrative functions required under the Protocol;
- Carrying out and maintaining inventory of laboratories with physical and human capacities to conduct research in modern biotechnology;
- Monitoring the activities of Institutional Biosafety Committees (IBCs) and Biosafety officers; l. building, equipping and maintaining offices and premises for the performance of its mandate under the Act;
- Carrying out capacity building activities in the regulation of modern biotechnology;
- Performing other duties as may be necessary for the full discharge of its functions under the Act; and
- Partnering with other relevant local and international agencies for the speedy realization of the Agency’s mandate.
To promote the basic tenets of biosafety as enunciated in the Cartagena Protocol on Biosafety and enforce Nigeria National Biosafety Regulatory Regimes to ensure the safe application and use of products of biotechnology
To ensure that the practice, process and procedures of modern biotechnology are undertaken within the limits of a regulatory systems that guarantees its safe use, protection of Nigeria’s biodiversity and with minimal risks to human health and environment.
The Core Values are:
- - Safety to the environment and human health;
- - Respect for human dignity;
- - Transparency;
- - Integrity
- - Professionalism
The National Biosafety Management Agency draws her powers from the NBMA Act 2015 which has given the Agency the power to act in her capacity to be responsible for providing regulatory framework, institutional and administrative mechanism for safety measures in the application of modern Biotechnology in Nigeria with the view to preventing any adverse effect on human health, animals, plants and environment and for related matters 2015 in accordance with the laws. Thus, the Agency is the national competent authority on all biosafety issues.
These concerns are not only peculiar to public interest groups and consumers, but to the NBMA as well. This is because, GM foods are officially new and with any new technology, there may be concerns.
But it is in the interest of the whole nation to know that no GM foods will be officially released into the market until they are confirmed safe by the NBMA and other relevant Agencies. So far, no GM food has been declared unsafe for human consumption (by WHO and FAO). Therefore, it is natural to be concerned about something one is not familiar with.
For enquiries, issues, clarifications and questions on biosafety in Nigeria, the Director-General/Chief Executive Officer can be contacted, through email to firstname.lastname@example.org or in person to the Planning, Research and Statistics Department of the Agency located at National Park Service Complex, Umaru Musa Yar’adua Way, Near City Gate, Abuja, www.nbma.gov.ng, +2348180805451.
Genetically Modified Organisms are plants, animals or microorganisms that have been altered genetically by the addition, deletion, or silencing of a gene for better performance of the recipient organism. The gene source could be from any organism not necessarily from a related species
The NBMA has given Permits to the following Institutions:
A. Confined Field Trails;
- Bio-fortified Cassava (increased levels of β-carotene & iron) at National Root Crops Research Institute (NRCRI), Umudike, Abia State.
- Africa Bio-fortified Sorghum (ABS) modified for decreased phytate levels and increased β-carotene, zinc & iron contents at Institute of Agricultural Research, Ahmadu Bello University, Zaria, Kaduna State.
- Pod-borer resistant cowpea at Institute of Agricultural Research, Ahmadu Bello University, Zaria, Kaduna State.
- Nitrogen Efficient Water Efficient Salt Tolerant (NEWEST) Rice at National Cereals Research Institute, Badeggi, Niger State.
- Monsanto Agriculture Nigeria Limited: CFT for Herbicide Tolerant Maize
- International Institute of Tropical Agriculture: GM cassava (AMY 3 RNAi Transgenic lines) modified for post-harvest starch reduction
- National Biotechnology Development Agency (NABDA): Herbicide Tolerant Soybean B. Commercial Release;
- BT cotton (insect resistance) C. Food, Feed and Processing;
- CHI Farms LTD: importation of soybean Genetically Modified for poultry feed processing.
- Agboola Farms: Soybean Genetically Modified for feed processing.
- Flour mills Nig. PLC: GM Maize for feed processing.
- ROM Oil Mills LTD: GM Soy bean for processing of edible oil.
Genetically Modified (GM) foods are those foods derived from GMOs as a whole, or ingredients.
This is not only a concern for the public but for NBMA as well. No GM foods will be allowed into Nigerian markets unless they are confirmed safe by the NBMA even if they are declared safe from the source, or country of origin.
For a GMO Permit to be granted to an individual or a corporation, the first step is to visit the NBMA website or the NBMA office to obtain appropriate guidelines and regulations for Terms and Conditions on any dealings on modern biotechnology and GMOs.
If it is a permit for modern biotechnology activity, then, the Facility will be required to be certified. If a permit is required for CFT, General Release (GR) or any other release, an appropriate application form should be completed and submitted to the NBMA. The NBMA will receive and process the application within 270 days after which a decision will be made and then be communicated to the applicant.
The NBMA Act 2015 empowers the Agency to regulate the application of modern biotechnology, with the view to preventing any adverse effect on human health, animals, plants and the environment, and any other related matters. The NBMA Act 2015 regulates GMOs for import and export. It generally regulates all trans- boundary movements of GMOs in Nigeria.
The Agency has staff that have been well trained both nationally and internationally on diverse biosafety related matters and has also established a state-of-the-art GMO Detection and Analysis Laboratory. In addition, the Agency has developed the following regulatory instruments to enhance its capability for its duties;
- The National Biosafety Management Agency Act 2015
- National Biosafety Policy
- National Biosafety Risk Analysis Framework
- GM Detection and Analysis Manual
- National Biosafety Application Administration Guidelines
- Biosafety Containment Facilities Guidelines
- Confined Field Trial Monitoring and Inspection Manual
- Biosafety Application forms
- Biosafety Laboratory Manual
- Decision Document
- National Biosafety Communication Strategy
- National Biosafety Emergency Response Strategy
- Biosafety Regulations
- GMOs Import, Export and Transit
- GMOs Packaging, Identification and Transport
- GMOs Commercial Release
- Biosafety Liability and Redress
- GMOs Contained Use and Confined Field Trial
Confined Field Trials (CFTs) are the on-farm, small-scale experimental phase of any GMO development process, with the intention of restricting genes and other genetic materials to the trial site. The trials are essential to ascertain the performance of the organism in the open, obtain safety data or other information. The restriction is to avoid the consumption of the organism and the persistence of the gene in the environment.
As an Agency, the NBMA has the responsibility of declaring a GMO safe for human consumption only after it carries out thorough analysis of that GMO called Risk Analysis.
Risk Analysis is a case-by-case scientific review of the safety issues associated with the GMO, history of its use, biological characteristics of the donor organism and the recipient organism, the magnitude of risk involved, the management measures of the risk, etc. to ensure there is no harm. For those GMOs for consumption, food safety analysis is carried out to ensure it is safe for consumption.
TThe NBMA as the Competent National Authority on Biosafety in Nigeria, has put in place measures to curtail the illegal importation of GM foods into the country. Individuals or corporations were given a time frame to apply for permits so as to make their importation official. For any GM food, it must be clearly labelled for ease of identification. The Agency sends, on regular basis, Biosafety Enforcement Officers to various super stores and markets for GMO suspect survey. This is to ensure total compliance. For non-compliance, a jail term, fine or both can be used to sanction any individual or corporation found guilty as specified in the NBMA Act 2015.
Furthermore, memoranda of understanding (MoU) have been signed amongst relevant border agencies for effective surveillance against illegal entry of GMOs into the country.
For any facility to be declared capable of carrying out genetic modification, the NBMA has to certify the facility.
The NBMA, in order to ensure public participation in decision making process, notifies the public using various channels of communication. The United Nations (UN) Biosafety Clearing House (BCH), NBMA website, Facebook and Twitter pages, publications in national and local newspapers, the NBMA Newsletter and the notice board in the NBMA office Complex are some media of public notice. The Annual Biosafety Conference is another medium.
The next step for GMOs in Nigeria is commercialization of more crops under trial, particularly those crops in the advanced stage of CFTs as the very first GMO, the BT cotton is almost getting into the Nigerian market.
These are words, acronyms or group of words that are mostly scientific, sometimes normal words that people use on daily basis but with different or slightly different meaning. Some of such are:
- GMOs: Genetically Modified Organisms
- CFTs: Confined Field Trials
- BCH: Biosafety Clearing House
- DNA: Deoxyribonucleic Acid
- RNA: Ribonucleic Acid
- LMOs: Living Modified Organisms
- Landraces: Varieties that are peculiar and available in a locality
- Facility: A laboratory, greenhouse or glasshouse where genetic modification takes place
- Gene transfer: Movement of genetic materials between two related species or varieties
- DIR: GMO dealings involving release
- DNIR: GMO dealings not involving release
- Containment: putting or placing under a four walled facility
- Confinement: putting in an open but restricted field, etc.