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.
South Korea: Navigating the Clinical Trial and Regulatory Environment - Webinar By GlobalCompliancePanel
27 March 2012, Wilmington, United States
Introduction
Venue
OnlineTraining
OnlineTraining, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
Related events
New Zealand Institute of Chemistry Conference 2024 (NZIC-24)
24 November 2024 14:00 - 28 November 2024 14:00, Dunedin, New Zealand
TAC 2025 - 60th Anniversary Conference
14 April 2025 09:00 - 16 April 2025 17:00, Guildford, United Kingdom
What's in that Perfume? - The Chemistry behind an iconic Christmas gift
3 December 2024 18:00-20:00, London, United Kingdom
Chemistry Teaching in Practice
9 January 2025 09:30-16:00, Oxford, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
