Introduction

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Japan. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in Japan. 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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• Further event details More information about the event

Venue

Online Training

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

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Organised by

GlobalCompliancePanel

Contact information

Mr webinars web
OnlineTraining, 1000 N West Street,, Suite 1200, Wilmington, 19801, United States of America
8004479407
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