Description
Job Description: Carry out Regulatory submission processes and Pharmacovigilance case processing within agreed timelines. Responsible for dossier preparation, review and compilation of documents required for submission of MA application in India. Responsible for dossiers compilation, preparation of briefing package for scientific advisory meetings and submission of BE NOC application, CDSCO NOCs, import permission, registration of products and/or sites in India. Responsible for applying Test li…
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