ComplianceOnline Announces Seminar on Life Sciences Regulations in China and Pacific Rim Countries
ComplianceOnline, the leading GRC advisory network, and respected life sciences regulations expert Robert J. Russell will conduct a two day seminar on compliance processes for life sciences products in China and the Pacific Rim markets.
- (1888PressRelease) August 23, 2012 - Palo Alto, CA, USA - ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on China & Pacific Rim Markets : Compliance Processes for Life Science Products - Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations. The two day seminar led by life sciences regulations expert Robert J. Russell will be held on September 13 and 14, 2012 in San Francisco.
This seminar will discuss the regulatory structure and requirements for compliance with in-country regulations for pharmaceuticals, medical devices, biologics and combination products in China and the Pacific Rim markets. This course has been pre-approved by RAPS and attendees will be eligible for up to 12 points towards their RAC upon completion.
For more information or to register for the seminar, please click here.
Seminar instructor Robert J. Russell is the President of RJR Consulting, Inc., which specializes in understanding global regulatory issues for the pharmaceutical industry. Mr. Russell has more than 25 years of experience working with FDA and the Commission on technical issues as they relate to policy development, regulation, clinical trial and the medical device development process.
During this interactive seminar, Mr. Russell will discuss the overall regulatory compliance requirements and procedures for life sciences products in China, Taiwan, Hong Kong, Singapore, Malaysia, Vietnam and Thailand. The course will cover topics relating to pre-clinical and clinical requirements as well as the structure of the regulatory agencies. Participants will also learn the methods by which regulators process filings and registrations and what is expected in the authorization and dossier maintenance of licensed products.
This course will be beneficial to the following personnel whose responsibilities require knowledge of Emerging Markets' regulatory requirements for life science products. Those who will particularly benefit from attending include Regulatory, Quality, Manufacturing, Global Business Development and General Management personnel whose responsibilities require local knowledge of regulatory, quality and import / export requirements. Administrative staff responsible for ensuring compliance with regulatory filings and overall GCP, GMP and GLP compliance requirements will also find this training highly relevant.
Date: Thursday, September 13 & Friday, September 14, 2012, 9 AM to 4 PM PDT
Venue & Location: Grand Hyatt, San Francisco, CA
Registration Cost: $899 per registration
Early bird discounts: For discounts on early registrations, please click here.
Register by phone: Please call our customer service specialists at +1-650-620-3937 or email to customercare ( @ ) complianceonline dot com
For more information on ComplianceOnline or to browse through our trainings, please visit our website.
About ComplianceOnline
ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 20,000 professionals from 3,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at http://www.complianceonline.com.
For more information please contact:
A Reuben Bernard
Manager of Program Marketing
ComplianceOnline
2600 E Bayshore Rd
Palo Alto CA USA 94303
650-620-3937 phone
650-963-2530 fax
reuben ( @ ) complianceonline dot com
http://www.complianceonline.com
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