Strengthening regulatory capacity for gene drives in Africa: Leveraging NEPAD's experience in establishing regulatory systems for medicines and GM crops in Africa

被引:17
|
作者
Glover B. [1 ]
Akinbo O. [2 ]
Savadogo M. [2 ]
Timpo S. [2 ]
Lemgo G. [3 ]
Sinebo W. [4 ]
Akile S. [4 ]
Obukosia S. [4 ]
Ouedraogo J. [3 ]
Ndomondo-Sigonda M. [1 ]
Koch M. [5 ]
Makinde D. [1 ]
Ambali A. [1 ]
机构
[1] NEPAD Agency, Industrialization, Science, Technology and Innovation Hub, Midrand
[2] African Biosafety Network of Expertise, Ouagadougou
[3] African Biosafety Network of Expertise, Dakar
[4] African Biosafety Network of Expertise, Kampala
[5] Simpot Plant Sciences, Boise, ID
关键词
New Partnership For Africa’s Development (NEPAD); Gene Drive Technology; Cartagena Protocol; Transgenic Mosquitoes; Confined Field Trials (CFT);
D O I
10.1186/s12919-018-0108-y
中图分类号
学科分类号
摘要
The New Partnership for Africa's Development (NEPAD) Agency recognizes that Africa is in a period of transition and that this demands exploring and harnessing safe advances made in science-based innovations including modern biotechnology. To advance the science of biotechnology in Africa effectively, while at the same time safeguarding human health and the environment, the African Union (AU) adopted a High-Level Panel report on modern biotechnology entitled, Freedom to Innovate, which advocated for a coevolutionary approach where technology development goes hand in hand with regulation. Furthermore, most AU member states are Parties to the Cartagena Protocol on Biosafety (CPB), a legally binding international agreement negotiated, concluded and adopted within the framework of the Convention on Biological Diversity. This seeks to guide Parties in developing systems for the environmentally sound management of modern biotechnology applications. Currently, 49 AU Member States have signed and ratified the CPB, of which 12 have passed biosafety laws. African Union (AU) member states are at different stages in the development of regulatory frameworks for applications of modern biotechnology, which include genetically modified (GM) products and other emerging technologies. Biosafety regulatory frameworks comprise: biotechnology and/or biosafety policy; laws, regulations and guidelines; administrative systems; decision-making systems; and mechanisms for public engagement. To assist Member States to implement functional regulatory frameworks for both agriculture and health applications, the NEPAD Agency established the African Biosafety Network of Expertise (ABNE) and the African Medicines Regulatory Harmonization (AMRH). Currently, transgenic insects and GM crops are regulated by Competent National Authorities whose mandate derives from national biosafety laws. For GM crops, a lot of research has been conducted up to the confined field trial (CFT) and multi-location trials stages in a number of African countries. Burkina Faso has fully functional containment facilities for transgenic mosquitoes while Mali and Uganda are developing theirs. The Burkina Faso regulatory agency has granted permits and has already received sets of sterile mosquito eggs for trials in the contained facility. It is instructive to note that both ABNE and AMRH have worked with national and regional regulatory bodies in Africa to enhance their technical capacities for informed decision making, adoption of best practices, and compliance with international standards. It is against the backdrop of a rich blend of on-the-ground knowledge, experience, expertise, and insight into the context and political sensitivities of member states that the NEPAD Agency seeks to expand existing support. This would include capacity strengthening in the regulation of emerging technologies, such as the application of gene drives in the development of transgenic mosquito for the control of malaria transmission. © 2018 The Author(s).
引用
收藏
相关论文
共 9 条
  • [1] Strengthening ethical and regulatory review capacity in Africa: unfinished business
    Nyika, A.
    TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2012, 17 : 77 - 77
  • [2] Establishing a regulatory value chain model: An innovative approach to strengthening medicines regulatory systems in resource-constrained settings
    Chahal, Harinder Singh
    Kashfipour, Farrah
    Susko, Matt
    Feachem, Neelam Sekhri
    Boyle, Colin
    REVISTA PANAMERICANA DE SALUD PUBLICA-PAN AMERICAN JOURNAL OF PUBLIC HEALTH, 2016, 39 (05): : 299 - 305
  • [3] Strengthening Blood Regulatory Systems to Tackle Africa's Unmet Needs for Blood and Blood Products
    Samukange, Washington T.
    Kafere, Chancelar
    Heinrich, Kristina
    Sabblah, George T.
    Siame, Mwewa M.
    Chirinda, Libert
    Reinhardt, Jens
    Hilger, Anneliese
    TRANSFUSION MEDICINE AND HEMOTHERAPY, 2023, 50 (02) : 123 - 128
  • [4] Medicines Regulatory Science Expertise in Africa: Workforce Capacity Development and Harmonisation Activities Towards the Establishment of the African Medicines Agency
    Bakani Mark Ncube
    Admire Dube
    Kim Ward
    Pharmaceutical Medicine, 2022, 36 : 83 - 97
  • [5] Medicines regulatory science expertise in Africa: Workforce capacity development and harmonisation activities towards the establishment of the African Medicines Agency
    Ncube, Bakani Mark
    Dube, Admire
    Ward, Kim
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2022, 31 : 660 - 660
  • [6] Medicines Regulatory Science Expertise in Africa: Workforce Capacity Development and Harmonisation Activities Towards the Establishment of the African Medicines Agency
    Ncube, Bakani Mark
    Dube, Admire
    Ward, Kim
    PHARMACEUTICAL MEDICINE, 2022, 36 (02) : 83 - 97
  • [7] Commercial Release of Genetically Modified Crops in Africa: Interface Between Biosafety Regulatory Systems and Varietal Release Systems
    Akinbo, Olalekan
    Obukosia, Silas
    Ouedraogo, Jeremy
    Sinebo, Woldeyesus
    Savadogo, Moussa
    Timpo, Samuel
    Mbabazi, Ruth
    Maredia, Karim
    Makinde, Diran
    Ambali, Aggrey
    FRONTIERS IN PLANT SCIENCE, 2021, 12
  • [8] The Adoption of Genetically Modified Crops in Africa: the Public's Current Perception, the Regulatory Obstacles, and Ethical Challenges
    Mmbando, Gideon Sadikiel
    GM CROPS & FOOD-BIOTECHNOLOGY IN AGRICULTURE AND THE FOOD CHAIN, 2024, 15 (01): : 1 - 15
  • [9] 5′-regulatory region of the goat α-s1-casein gene drives tissue-specific expression of highly active human G-CSF and GM-CSF proteins in the mammary gland of transgenic mice
    Burkov, Ivan
    Serova, Irina
    Dvoryanchikov, Gennady
    Andreeva, Lyudmila
    Battulin, Nariman
    Smirnov, Alexandr
    Serov, Oleg
    TRANSGENIC RESEARCH, 2011, 20 (05) : 1153 - 1153