Global Regulatory Management (GRM) is a company specializing in the management of pharmaceutical regulatory affairs. It was created in 2018 by 2 partners who each have 20 years of experience in the pharmaceutical industry (in France, the USA and in sub-Saharan Africa), during which they held Market Access, Sales, Marketing and Director positions. general in reputable multinationals (GSK, Sanofi, Pfizer, Roche and Sandoz). GRM currently covers 15 territories of French-speaking sub-Saharan Africa which are: Benin, Burkina Faso, Cameroon, Central African Republic, Democratic Republic of Congo, Cote d'Ivoire, Gabon, Guinea, Mali, Mauritania, Niger, Senegal, Chad, Togo. These countries represent around 600 million Euros of the pharmaceutical market and are part of common regional political and economic groups. However, despite progress, the procedures for obtaining Marketing Authorization (Marketing Authorization) are not harmonized, making the processes diverse and complex. Thus, GRM's mission is to manage and facilitate the process of obtaining MA for the count of pharmaceutical companies in compliance with the compliance dictated by the code of good practice of the IFPMA. We provide: • The constitution of application files for MA (Registration) and post MA (Renewal / Variation). • The follow-up of MA applications, the response to questions from the administrations and the collection of the necessary additions. • The follow-up of new requests under investigation and export registration files. • Filing of AMM files. • Archiving of marketing authorization files and regulatory information. Thanks to its good reputation, its image of excellence and its uniqueness of value proposition, we have a portfolio of loyal and long-standing clients, continuously reinforced by new clients eager to penetrate the French-speaking Sub-Saharan Africa market. We are confident that our diverse and complementary core competencies will bring long-term success to our customers.