Webinar on South Korea: Navigating the Clinical Trial and Regulatory Environment

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Jun 14 - 14, 2016
In-person

Why Attend

Overview:

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.

Agenda of the Session:

Overview of South Korea's Healthcare System
- South Korea’s Regulatory Agencies Structure and Responsibilities
- South Korean Drug Development Process
Agency Review Process for Decision-Making
- Country Establishment Licensing & Procedures
- South Korea and ICH (International Conference on Harmonization)
Requirements for Clinical Trials in South Korea
- The Changing KFDA
- Product Labeling Requirements
- Cultural Aspects - Working in South Korea
- Effectively working with the Regulators; Do's and Don'ts, Practical Experiences Shared

Learning Objectives: This course is designed to provide an overview of the regulatory environment in South Korea and will provide training in:

What is the Regulatory Structure in South Korea
Understanding the specific procedures for Pharmaceutical Products
How to begin your company involvement in South Korea
Requirements for Clinical Trials in South Korea
South Korean Drug Development Process
The Changing KFDA
Understanding the Local Culture: How to negotiate with the regulators

Who will benefit: This course will be of benefit to regulatory personnel whose responsibilities require knowledge of South Korea's regulatory environment. Administrative staff responsible for ensuring compliance with regulatory filings and overall regulatory compliance requirements will also find this training highly relevant. Any sales or general management employee requiring an understanding of how regulations and compliance issues impact the organization will also benefit.

Speaker Profile:
Robert J. Russell For the past 9 years, Bob has been President of RJR Consulting, Inc. The company assists the pharmaceutical, medical device and biotech industries in understanding and complying with International Regulations affecting compliance, new product development, manufacturing and quality assurance. RJR has offices in Columbus, OH, Washington, DC, Brussels, Belgium with exclusive affiliates across Asia and Latin America. Bob has 28 years of past industry experience as a CMC specialist, R&D Director and Global Director of Regulatory Affairs for Merion Merrill Dow pharmaceuticals and Cordis-Dow medical devices. He has a BS / MS degree in Chemistry.

Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
Event Link : http://bit.ly/Regulatory_Environment
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