Work from Office
Full Time
Preparation, Review and Submission of documents related to Product registration with CDSCO and FDCA.
Review of the Regulatory applications for Emerging Markets (ROW).
Preparation, Review and Submission of applications for Manufacturing License.
Preparation, Review and Submission of applications for Registration of GMP Certificates (WHO-GMP, State GMP), COPP, FSC certificate etc.
Co-ordination with various departments related to the Regulatory Submissions with respective teams i.e., F&D, QC, Production and QA.
CONCORD
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