Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales:	Glover, Barbara, Akinbo, Olalekan, Savadogo, Moussa, Timpo, Samuel, Lemgo, Godwin, Sinebo, Woldeyesus, Akile, Sunday, Obukosia, Silas, Ouedraogo, Jeremy, Ndomondo-Sigonda, Margareth, Koch, Muffy, Makinde, Diran, Ambali, Aggrey
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069767/ https://www.ncbi.nlm.nih.gov/pubmed/30079102 http://dx.doi.org/10.1186/s12919-018-0108-y

Ejemplares similares

Commercial Release of Genetically Modified Crops in Africa: Interface Between Biosafety Regulatory Systems and Varietal Release Systems
por: Akinbo, Olalekan, et al.
Publicado: (2021)

Relevance of Crop Biology for Environmental Risk Assessment of Genetically Modified Crops in Africa
por: Akinbo, Olalekan, et al.
Publicado: (2015)

Problem formulation for gene drive mosquitoes designed to reduce malaria transmission in Africa: results from four regional consultations 2016–2018
por: Teem, John L., et al.
Publicado: (2019)

Medicines Regulation in Africa: Current State and Opportunities
por: Ndomondo-Sigonda, Margareth, et al.
Publicado: (2017)

A new approach to an old problem: Overview of the East African Community’s Medicines Regulatory Harmonization initiative
por: Ndomondo-Sigonda, Margareth, et al.
Publicado: (2020)

Best practices in the African Medicines Regulatory Harmonization initiative: Perspectives of regulators and medicines manufacturers
por: Ndomondo-Sigonda, Margareth, et al.
Publicado: (2023)

National medicines regulatory authorities financial sustainability in the East African Community
por: Ndomondo-Sigonda, Margareth, et al.
Publicado: (2020)

Optimizing the East African Community’s Medicines Regulatory Harmonization initiative in 2020–2022: A Roadmap for the Future
por: Arik, Mawien, et al.
Publicado: (2020)

Harmonization of medical products regulation: a key factor for improving regulatory capacity in the East African Community
por: Ndomondo-Sigonda, Margareth, et al.
Publicado: (2021)

Coming together to improve access to medicines: The genesis of the East African Community’s Medicines Regulatory Harmonization initiative
por: Sillo, Hiiti, et al.
Publicado: (2020)

Evaluation of the Effectiveness and Efficiency of the East African Community Joint Assessment Procedure by Member Countries: The Way Forward
por: Ngum, Nancy, et al.
Publicado: (2022)

Evaluation of the effectiveness and efficiency of the East African community joint assessment procedure by pharmaceutical companies: Opportunities for improvement
por: Ngum, Nancy, et al.
Publicado: (2022)

A rapid assessment of the National Regulatory Systems for medical products in the Southern African Development Community
por: Dube-Mwedzi, S., et al.
Publicado: (2020)

Evaluation of no evidence of progression or active disease (NEPAD) in patients with primary progressive multiple sclerosis in the ORATORIO trial
por: Wolinsky, Jerry S., et al.
Publicado: (2018)

Expanding global access to essential medicines: investment priorities for sustainably strengthening medical product regulatory systems
por: Roth, Lukas, et al.
Publicado: (2018)

Mapping the regulatory landscape of AI in healthcare in Africa
por: Townsend, Beverley Alice, et al.
Publicado: (2023)

The governance of genomic biobank research in Africa: reframing the regulatory tilt
por: Staunton, Ciara, et al.
Publicado: (2020)

Eight years of the East African Community Medicines Regulatory Harmonization initiative: Implementation, progress, and lessons learned
por: Mashingia, Jane H., et al.
Publicado: (2020)

Mycotoxin Regulatory Status in Africa: A Decade of Weak Institutional Efforts
por: Chilaka, Cynthia Adaku, et al.
Publicado: (2022)

Needs‐driven talent and competency development for the next generation of regulatory scientists in Africa
por: Semete‐Makokotlela, Boitumelo, et al.
Publicado: (2021)

The role of corruption control and regulatory quality in energy efficiency transition tendencies in Africa
por: Akorli, Charity Dzifa, et al.
Publicado: (2023)

The Regulatory Review Process in South Africa: Challenges and Opportunities for a New Improved System
por: Keyter, Andrea, et al.
Publicado: (2018)

Evaluation of the Performance of the South Africa Regulatory Agency: Recommendations for Improved Patients’ Access to Medicines
por: Keyter, Andrea, et al.
Publicado: (2019)

Biosafety Regulatory Reviews and Leeway to Operate: Case Studies From Sub-Sahara Africa
por: Komen, John, et al.
Publicado: (2020)

Assessment of the effectiveness and efficiency of the West Africa medicines regulatory harmonization initiative by the member countries
por: Owusu-Asante, Mercy, et al.
Publicado: (2022)

Strengthening Blood Regulatory Systems to Tackle Africa's Unmet Needs for Blood and Blood Products
por: Samukange, Washington T., et al.
Publicado: (2022)

Ethical, Regulatory and Market related aspects of Deploying Triple Artemisinin-Based Combination Therapies for Malaria treatment in Africa: A study protocol.
por: Tindana, Paulina, et al.
Publicado: (2021)

Nursing and midwifery regulatory reform in east, central, and southern Africa: a survey of key stakeholders
por: McCarthy, Carey F, et al.
Publicado: (2013)

Regulatory and policy implications of sand mining along shallow waters of Njelele River in South Africa
por: Gondo, Tendayi, et al.
Publicado: (2019)

Regulatory standards and guidance for the use of health applications for self-management in Africa: scoping review protocol
por: Bene, Benard Ayaka, et al.
Publicado: (2022)

Editorial: Dentistry and oral health in Africa
por: El Tantawi, Maha, et al.
Publicado: (2023)

Impact of regulatory requirements on medicine registration in African countries – perceptions and experiences of pharmaceutical companies in South Africa
por: Narsai, Kirti, et al.
Publicado: (2012)

Historical Perspectives on Ethical and Regulatory Aspects of Human Participants Research: Implications for Oncology Clinical Trials in Africa
por: Salhia, Bodour, et al.
Publicado: (2020)

Corrigendum: Regulatory and policy implications of sand mining along shallow waters of Nzhelele River in South Africa
por: Gondo, Tendayi, et al.
Publicado: (2019)

The role of environmental regulatory quality in the relationship between natural resources and environmental sustainability in sub-Saharan Africa
por: Oteng-Abayie, Eric Fosu, et al.
Publicado: (2022)

Regulatory registration timelines of generic medicines in South Africa: Assessment of the performance of SAHPRA between 2011 and 2022
por: Moeti, Lerato, et al.
Publicado: (2023)

Sub-optimal satisfaction of people living with HIV and AIDS regarding their care in Burkina Faso, West Africa
por: OUÉDRAOGO, SMAÏLA, et al.
Publicado: (2023)

Ethical reasoning and participatory approach towards achieving regulatory processes for animal-visitor interactions (AVIs) in South Africa
por: Muzzo, Alessia, et al.
Publicado: (2023)

Funding and financial sustainability of pharmacovigilance: suggested models for funding pharmacovigilance in resource-limited African countries
por: Isah, Ambrose O., et al.
Publicado: (2023)

Information and communication technology development and health gap nexus in Africa
por: Megbowon, Ebenezer Toyin, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_g2o7urmv3vpa26le9cpo0naqvj