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Comprehensive overview of FDA procedures, marketing authorisation requirements, and recent developments in drug approval process. Best course offering practical insight into requirements, latest developments, submission procedures, and regulatory changes. Suitable for regulatory affairs personnel, lawyers, and those preparing US registration documents.
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Timings09:00 AM-06:00 PM (expected)Not Verified | Entry FeesPaid Ticket Check Official Website |
Estimated Turnout500 - 1000 Delegates Based on previous editions | Event TypeConference |
EditionsDec 2024 Interested+14 more editions Frequency Bi-annual | Official LinksWebsiteContacts Report Error Claim this event |
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