March 28-30, 2017 • Bethesda North Marriott • North Bethesda, MD
The Annual Medical Device Quality Congress is going strong on their 14thyear. The conference will be located at the Marriott Bethesda North Hotel & Conference Center in Bethesda, MD on March 28-30, 2017. The FDAnews global compliance company presents the event and offers workshops, panels and presentations by industry experts, med tech business leaders and regulatory officials. FDAnews will host over 1,800 attendees at this event, making it a key event for medical device and professionals.
Grace Fu Palma, founder of China Med Device will be speaking at the event at 3:45 on Wednesday, March 29. The panel, “China CFDA Medical Device Pre-Market Approval and Post Market Quality Regulatory System Overview” will discuss the most recent changes to the China Food and Drug Administration. Grace will highlight some of the challenges facing both manufacturers in domestic and multinational markets in China today.
There will be many key speakers from the FDA, as well as industry and company leaders. The Center for Devices and Radiological Health (CDRH), will lead discussions around premarket approvals, safety, and manufacturing for the medical device industry. They will discuss the top strategies and priorities for 2017. This will be a compelling presentation because the CDRH is an agency within the FDA that is liable for premarket approval of medical devices. Other presentations will include benefit-risk considerations for medical devices, quality defining industry metrics, and FDA cybersecurity for medical devices. The FDA will also communicate their compliance guidelines and information regarding the new administration, lawmakers and regulators, and what that means for U.S. and European and Chinese medical device markets.
The Medical Device Quality Congress is an annual event. It is a key event for the medical device industry in 2017. Attendees will have the chance to:
- Listen to FDA leaders and officials lay out goals & plans for 2017
- Hear about the MDSAP pilot program and lessons learned.
- Discuss what the new President has prepared for the FDA under his administration.
- Learn strategies from industry experts, consultants and lawyers, people who’ve improved relations with FDA to work towards successful marketing and manufacturing of medical devices.
- Listen to case study examples where people have recognized compliance issues and found efficient and cost effective solutions before the issue turned into a catastrophe.
This conference is imperative for those in management levels in the medical device industry. It will be beneficial to those involved in medical device regulation, R&D, consulting, manufacturing and risk management. For more details on the annual conference, click here.
To discover how China Med Device services companies of all sizes and unique situations with information and strategies regarding entering the China medical device market and complying with CFDA regulations in China, call us in the U. S. at 978-390-4453, in China at 18201749732, or email us at email@example.com.