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Introduction

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceutical Products in South Korea. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in South Korea. Content will also include descriptions of the methods by which regulators in the corresponding agencies process filings and registrations and what is expected in the authorization and dossier maintenance of licensed products.

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Venue

OnlineTraining

OnlineTraining, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr webinar web
online training webinar, 1000 N West Street, Suite 1200, Wilmington,DE, 19801, United States of America
8004479407
Contact us by email

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