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MAIN ACTIVITIES FOR THE JOB Contribute to regulatory activities performed on the RA Platform/the Hub. Regulatory activities include pre licensing activities, new registration (sites and medicinal products), post licensing regulatory submissions, interaction with health authorities on
Senior Regulatory Affairs Consultant Key Responsibilities Global Regulatory Submissions & Lifecycle Management Lead the preparation, compilation, review, and submission of regulatory dossiers to global health authorities including US FDA, EMA, MHRA, TGA, HSA, NPRA, Thai FDA, Taiwan
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