Palo Alto, California (PressExposure) August 21, 2012 -- ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on Global Medical Device Regulations - US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, Taiwan. The one and a half day seminar led by regulatory affairs expert Dr. David Lim will be held on September 13 and 14, 2012 in Minneapolis.
This seminar will discuss the medical device regulations of 12 countries including United States, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea and Taiwan. This course has been pre-approved by RAPS and attendees will be eligible for up to 10 points towards their RAC upon completion.
For more information or to register for the seminar, please click here.
Seminar instructor Dr. David Lim obtained his Ph.D. in biological sciences at the University of Missouri-Columbia. Since then, Dr. Lim has held various positions at Duke, US National Laboratories, Intrexon Corporation, Terumo, US FDA/CDRH, and EraGen Biosciences, Inc., a Luminex Company. Currently, Dr. Lim is serving as a faculty at the Regulatory Affairs Professional Society (RAPS) and is an advisor to the Presidents and CEOs of FDA-regulated industry.
During this interactive seminar, Dr. Lim will discuss medical device regulations of 12 countries concerning medical devices, active implantable medical devices and in vitro diagnostic medical devices for adequate implementation and successful registration. Participants will also gain a thorough understanding of ISO 13485, ISO 14155, ISO 14971, GHTF documents, and MEDDEV guidance documents for quality and adverse event reporting including group discussions facilitating interpretation, understanding, and implementation of medical device regulations.
This seminar will be valuable for anyone in the European Commission (EC) and FDA-regulated industry, including, but not limited to, medical devices, active implantable medical devices, in vitro diagnostic medical devices or combination products. It will be beneficial to those involved in research and product development, handling data and documents for regulatory submission for CE-marking purposes, conducting/monitoring/coordinating clinical investigation, and/or performing risk management and post-market vigilance/surveillance. This workshop is a must for those who are directly or indirectly involved in drafting and handling applications for CE marking purposes.
Date: Thursday September 13, (9 AM to 4 PM CDT) & Friday September 14, (8 AM to 12 Noon CDT)
Venue & Location: Hyatt Regency Minneapolis, MN
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 firstname.lastname@example.org
For more information on ComplianceOnline or to browse through our trainings, please visit our website.
For more information please contact:
A Reuben Bernard
Manager of Program Marketing
2600 E Bayshore Rd
Palo Alto CA USA 94303