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Head of RA and Medical Affairs

Head Regulatory and Medical Affairs Lead and manage the registration process in ensuring approvals of new products, manufacturing permits, import permits and amendments to products in the 3 countries. Contact with health authorities on regulatory conditions. Manage all Regulatory, Pharmacovigilance, Quality, Medical, Compliance & Publicity activities in the 3 countries. Monitor pharmaceutical laws and ensure operational compliance (advertising, congress, packaging, samples, pharma SOP,...). Lead a multi-country team of regulatory affairs, medical and quality experts.

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