Because of complex product safety standards, many countries require medical device manufacturers to have a third-party audited and certified management system in place before selling any medical product. Companies are coming to the realization that designing and manufacturing their product for regulatory compliance is critical to the development of innovative healthcare solutions as they face the challenges of rapidly evolving regulations and increased regulatory scrutiny.
To better position medical device companies to excel in this evolving market, Intertek, a global third party testing and certification company, invites you to attend their upcoming webinars. Their “Navigating Regulatory Compliance within the Medical Device Industry” webinar series will address a unique aspect of the compliance process for medical devices, management systems, chemicals and pharmaceuticals.
Oct. 1, 2013, at 2 p.m. U.S. EST
Common Pitfalls and Best Practices for 3rd Edition Risk Management
Oct. 24, 2013 at 2 p.m. U.S. EST
Home Healthcare, 60601-1-11 Series Review
Oct. 30, 2013, at 2 p.m. U.S. EST
The First Amendment to the Third Edition, Simplified
Nov. 6, 2013, at 2 p.m. U.S. EST
All You Need to Know About RoHS 2
Nov. 13, 2013, at 2 p.m. U.S. EST
Navigating Risk for 61010-1, Third Edition