What is the Regulatory Structure in Japan 2018

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Category Japan, Combination Products, Compliance Processes for Life Sciences, Regulatory Filing Requirements, Compliance fda courses, Risk Management, Labelling Requirements

Deadline: June 10, 2018 | Date: June 13, 2018

Venue/Country: Online, U.S.A

Updated: 2018-04-18 15:36:07 (GMT+9)

Call For Papers - CFP

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.

Agenda:

Japan's Regulatory Structure for the Life Science Product Industries

Demographic

Regulatory Framework: Key Agencies Involved / Reporting Structure

MHLW (Ministry of Health, Labour and Welfare)

PMDA (Pharmaceutical and Medical Device Agency)

PAFSC (Pharmaceutical Affairs and Food Sanitation Council)

Who Will Benefit:

Regulatory Personnel whose responsibilities require knowledge of Japan's regulatory environment

Administrative staff responsible for ensuring compliance with regulatory filings and overall regulatory compliance requirements will also find this training highly relevant

Speaker Profile:

Robert J. Russell For the past 9 years, He 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.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com