Sr Exe

Year Vadodara, Gujarat, India

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Compilation , review of dossier for US , EU , AU, Canada & IL market for both solid oral and non-oral dosage form
Review of query response prepared and compiled by regulatory associates
Manage all the activities pertaining to dossier submission for aforesaid markets .
Meet the dossier submission and query response timeline as per given target
Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management
Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
Lifecycle management for US , EU, Canada & IL market
Single point contacts for all the regulatory submission activities for IL and Palestine markets

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