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To study and update Regulatory guideline of assigned countries and to prepare checklist / template for registration dossier.
鈥� To verify specification of excipients , active , finished product and packaging material and all required documents.
鈥� Application, review, co-ordination, follow-up of legal documents COPP , FSC etc.
鈥� Maintain Proper database w.r.t to master document dossier.
鈥� To collect and verify all technical documents and information from various departments at the manufacturing site
鈥� To prepare and compile registration dossier as per the guidelines and checklist and submit to marketing to further submission to regulatory authorities.
鈥� Regulatory support to va...

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