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Latest in Regulatory

  • October 5, 2026

Burkina Faso launches Faso FDA with new leadership

The government of Burkina Faso has formally installed the first leaders of Faso Food and Drug Administration (Faso FDA), a new agency created by merging the national...

By Drug Eye Africa Newsroom
  • September 30, 2026

Mozambique’s ANARME shuts Maputo medical clinic over pharmaceutical irregularities

The Autoridade Nacional Reguladora de Medicamentos has suspended Clínica Médica de Maputo with immediate effect after finding expired medicines, products with Mandarin labelling of unverified regulatory status,...

By Drug Eye Africa Newsroom
  • September 30, 2026

Morocco’s AMMPS opens applications for clinical trial site accreditation

The Agence Marocaine du Médicament et des Produits de Santé has begun accepting accreditation applications for sites conducting clinical trials of experimental medicines and clinical investigations of...

By Drug Eye Africa Newsroom
  • September 30, 2026

Cape Verde’s ERIS marks ten years of cosmetics regulation

The Entidade Reguladora Independente da Saúde has marked ten years since Decree-Law 21/2016 established Cabo Verde's first legal framework for cosmetic products, with market supervision gradually strengthened...

By Drug Eye Africa Newsroom
  • September 29, 2026

Botswana’s BoMRA opens voluntary notification for Class A medical devices

The Botswana Medicines Regulatory Authority has opened a voluntary notification registration period for Class A medical devices, including in vitro diagnostics, veterinary devices and dental consumables, running...

By Drug Eye Africa Newsroom
  • September 27, 2026

Tanzania’s TMDA joins Medical Device Single Audit Program as affiliate member

The Tanzania Medicines and Medical Devices Authority has become an affiliate member of the Medical Device Single Audit Program, gaining access to international audit reports and manufacturer...

By Drug Eye Africa Newsroom
  • September 25, 2026

ANAMEV trains technical staff on medicine marketing authorisation evaluation

The Agence Nationale des Médicaments et des Évacuations Sanitaires has held a four-day internal training for its technical team on evaluating marketing authorisation dossiers, as mandatory registration...

By Drug Eye Africa Newsroom
  • September 25, 2026

ANAMEV publishes procedure for submitting marketing authorisation applications

The Agence Nationale des Médicaments et des Évacuations Sanitaires has published guidance on how to submit marketing authorisation applications, including two submission channels, fee requirements and reception...

By Drug Eye Africa Newsroom
  • September 25, 2026

Morocco’s AMMPS updates batch release checklist for vaccines and sera

The Agence Marocaine du Médicament et des Produits de Santé has updated the checklist for batch release applications for vaccines and sera, effective 22 September 2026, clarifying...

By Drug Eye Africa Newsroom
  • September 25, 2026

ANARME recovers state-owned medicines and equipment from private health facility in Nampula

Mozambique's medicines regulator has recovered state-owned medicines, medical materials and hospital equipment from a private health facility in Nampula city, detaining one person suspected of illegal possession...

By Drug Eye Africa Newsroom

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