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Looking to integrate african Market?

We Simplify  Registrations

Our Services

  • Product development

  • Global Chemistry, Manufacturing & Control (CMC) and Global Regulatory affairs

  • Product promotion / Sub-saharan Africa

  • Pharmacovigilance

  • Translation English / French

Product development

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  • Support / advice for regulatory compliance

  • Advice on designing clinical trials and choosing investigator

  • Clinical trial and application

  • Coordination of clinical trials

  • Writing patient Information Leaflet (PIL) and Summary of Product Characteristics (SmPC)

Global Chemistry, Manufacturing & Control (CMC) and Global Regulatory affairs (RA)

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  • Writing all CMC documentation for registration dossiers (CTD)

  • Compilation of CTD and management of all regulatory submissions (particularly for Africa market)

  • Follow – up all regulatory process (particularly for Africa market)

  • Management of product life cycling (particularly for Africa market)

  • Global regulatory intelligence

Promotional Activities / Sub-saharan Africa

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  • Market access consultation

  • Local representation and promotional activities

  • Pricing and public sector reimbursement analysis

  • Management / advice on public markets

  • Market targeting and survey and penetration

Pharmacovigilance

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  • Management of Individual Case Safety Report (ICSR)

  • Management and reporting of all post-marketing information

Documents Translation

  • English / French

In the past, we spent much of our time building our product registration records. Today, we are saving  time with the services of Afrobridge Pharma.
The recordings of our products in Africa have become simpler.

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Xavier Lambert.

CEO Mundo Pharma;

Since our collaboration with Afrobridge Pharma, our dossiers are filed in time and we get more quickly the marketing authorizations of our products in Africa

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Alice Mercier. 

Registration Manager, AIK Health.

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