organized by complianzworld 2014 - Global Medical Device Regulations: US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, Taiwan: One and a Half-day In-person Seminar

Description:
Understanding global medical device regulations and requirement and adequate implementation of applicable medical device regulations can significantly expedite the regulatory processes, bringing innovative medical products to the global market faster and saving enormous amount of your unnecessary time, efforts and investment.
At this workshop, you will get familiar with medical device regulations of twelve (12) countries concerning medical devices, active implantable medical devices and in vitro diagnostic medical devices for adequate implementation and successful registration.
Target Audience:
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. This seminar will be particularly useful for 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.
Price Tags:
$ 1399 Seminar - Single registration (Earlybird Price)
$ 6396 Special - Group Discount; Register for 5 attendees
Please reach us at +1-866-978-0800 for any further assistance or if you wish to register.