In an era where medical device regulation globally is changing faster than ever before, can you afford not to be up-to-date with current and upcoming changes?
Save the date to find out what's next for medical device regulations: November 28-29, 2012.
The program will deliver practical guidance on today’s pressing issues:
• Comprehensive guidance to the changes proposed to the European Medical Device Directives, the timetable for future changes and an examination of what will replace the Global Harmonisation Task Force
• Achieve clarification over the challenges in the US regarding 510 (k) submissions in light of the IoM decision
• Overcome the varied challenges of clinical requirements and prepare your response to the changing interpretation of the clinical requirements following 2007/47/EC
• Develop a globally applicable strategy to boost your market reach in India, Brazil, China and the Middle East, with practical and regulatory insights from our interactive panel discussion with industry thought leaders
• Plus an interactive workshop on how to deal effectively with Notified Bodies
