Webinars will cover medical device approval and quality system requirements in the Brazilian and Japanese markets.
Online PR News – 20-September-2011 – – Emergo Group, an Austin, Texas-based medical device regulatory consulting firm, is conducting a series of webinars over the coming months explaining the medical device registration process in Brazil and Japan.
Although Brazil and Japan represent two of the world’s largest medical device markets, regulatory requirements for commercialization in these countries can prove challenging for foreign manufacturers. Emergo Group’s webinars will provide information on the ANVISA medical device registration process in Brazil, and the PMDA medical device approval and certification process in Japan.
Quality management system issues including Brazilian Good Manufacturing Practices and Japan’s MHLW Ordinance #169 requirements will also be covered in the Emergo Group webinars, as well as device classification, authorized representation and other relevant topics.
Webinar dates and registration instructions can be found below:
How to Get a Medical Device Approved for Sale in Brazil
September 27, 2011
The Medical Device Approval Process in Japan
October 18, 2011
About Emergo Group
Emergo Group is a global medical device consulting firm providing a wide range of services for device registration, QMS compliance, clinical trial management, in-country representation, reimbursement and distributor search consulting.
Regulatory Editor, Emergo Group