Global Medical Device Focus 2021: China & Taiwan
Event Information
About this event
Global Medical Device Focus 2021
Come join the medical device industry's leading experts and authorities in global clinical research and regulatory affairs for an exciting program of discovery and exchange. With a diverse array of topics and discussions to choose from, there's something for everyone at the Global Medical Device Focus 2021. This great opportunity will help participants learn what it takes to successfully plan, implement, and obtain successful medical device registrations throughout various countries and regions around the world.
Business & Regulatory: Discover how you can optimize revenue by planning early for your medical device global market access.
Clinical Evaluation: How to conduct global clinical investigations? Learn what data is needed to access world markets including China.
Live Q&A sessions: You've got the questions; we have the answers!
Event: Global Medical Device Focus 2021: China & Taiwan
Date: September 9, 2021
Time: 11:00am – 13:30pm CET
Program:
• Latest Update on Market Access Requirements in China
Steven Wen
• Conducting Clinical Investigations in China
Li Xin, MD-CLINICALS
• Conducting Clinical Investigations in Taiwan
Ivon Septriyana, MD-CLINICALS
• Taiwan Medical Device Regulatory Requirements Update
Jenny Lin, Brandwood CKC
• Market Entry Considerations for Mainland China
Maxime Van 't Klooster, Acclime
• Q&A session
For more information about Global Medical Device Focus 2021 or to see all other upcoming live webinar events, be sure to visit: www.globalmedicaldevicefocus.com
Don't miss this great Global Medical Device Focus 2021 webinar, register today!
September 16, Middle East: https://gmdf2021-middle-east.eventbrite.ch
November 22, South America: https://gmdf2021-south-america.eventbrite.ch
Organizer MD-Clinicals
Organizer of Global Medical Device Focus 2021: China & Taiwan
With over 30 years of experience in managing medical device clinical investigations around the globe, MD Clinicals has what it takes to move your product to market swiftly and cost-effectively, saving you precious time and money in the process.
Our unsurpassed clinical and regulatory expertise in medical device market access combined with rigorous anticipatory approach and strong communication means you avoid the unnecessary delays and unexpected problems that affect eight out of ten clinical trials in the world today.