TÜV SÜD, a member of MassMEDIC, will be holding three intensive workshops for medical device manufacturers and suppliers on the following topics:
The third edition of IEC 60601-1 mandates that medical device manufacturers manage risk throughout their supply chains. When the third edition of IEC60601-1 was published, it marked the beginning of a new era. The standard now incorporates the concept and application of risk management in the design and production of devices. Join TÜV SÜD for our Risk Management Workshop on September 30, 2013, in Boston. To register, visit http://tuvamerica.com/tuvnews/seminars/seminarinfo.cfm?id=199
CAPA is one of the most challenging quality system elements that companies face during inspections and audits. To help quality professionals address these challenges, TÜV SÜD has developed a comprehensive training program. The training program includes a one-day workshop and access to three recorded webinars. To register for the CAPA Workshop on September 30, 2013, in Boston, visit http://tuvamerica.com/tuvnews/seminars/seminarinfo.cfm?id=201.
Get first-hand information of all the regulatory updates (Brazil, ASEAN, Russia, India, China, Japan and EU). Meet with management, experts and your local auditors. There are currently 80 attendees so there will be plenty of Networking and Expert Table Discussions! To register for our annual International Regulatory Update, visit http://tuvamerica.com/tuvnews/seminars/seminarinfo.cfm?id=192.
All MassMEDIC members will receive a discounted registration rate of $595 per attendee. Enter massmedic in the promotion code box in the registration to qualify for this $200 discount. Additional discount available for two or more attendees, please contact Robert Dostert, Director, Business Development and Sales, TÜV SÜD America Inc., 978 530 7986 or email firstname.lastname@example.org. Onsite training is also available for five or more students.