We are pleased to announce Grace Fu Palma, CEO of China Med Device, LLC, was selected to chair the opening panel of China Regulatory and Reimbursement Environment during The MedTech Conference powered by Advanced Medical Technology Association (AdvaMed).
The China Regulatory & Reimbursement Forum will take place from 9:15 AM – 12:15 PM on Tuesday, September 25, 2018 in PCC – Room 204A in Philadelphia. Grace Fu Palma will join other public and private stakeholders from China and the U.S. to discuss the latest trends and changes in China CFDA regulations and reimbursement and how they impact MedTech industries in the Western countries.
The MedTech Conference is the premier, global event convening approximately 3,000 participants from over 1,000 of the leading, worldwide innovators in medical devices, diagnostics and health information systems.
During the China Regulatory CFDA Session – Era of Transformation, Grace Fu Palma will provide an overview of CFDA’s Major Restructuring and Updates in 2018. Lindsay Tao, Corporate Director, Global Health Policy, Johnson & Johnson Corporate will talk about the overview of Recent Clinical Requirement Changes and Looking Ahead to 2019. Other panel members are Nicole Taylor Smith, JD Senior Director, Global Regulatory Affairs Policy and Intelligence, and Michael Edward Pfleger, VP, Alcon Laboratories, Inc.
Following the regulatory session, Stephen Hull, Founder, Hull Associates LLC, will moderate the China Reimbursement & Payment Session. Topics covered are the overview of China’s public and private reimbursement and payment system, and key processes to obtain charge code approval and reimbursement codes for new devices. Speakers invited are Yingyao Chen, Professor of Health Services at the School of Public Health, Fudan University (FUSPH), Lynn Jiao, Vice President & China Executive Director, AdvaMed, and Guilin Zhan M.D. Professor and Head of Dept. of International Affair of Huaxia Eye Hospital Group, Xiamen, China
Grace fu Palma, a Sino-US MedTech veteran, founded China Med Device to provide turn-key solutions for western medical device/IVD companies to enter China with regulation and commercialization services. She has been a speaker at national regulatory meetings as well as column contributor for US regulatory news and journals. With 20+ years of experience driving global product strategy, commercialization, partnerships, and China operations for both large multinationals and startup companies, she has held a variety of management positions in marketing and operations at multinationals and start-ups.
China Med Device will be exhibiting at the MedTech Conference. Please visit at Booth #203 in the exhibition hall. Also, please contact info@ChinaMedDevice.com to schedule your meeting or request more information.
We are honored to invite you to join our panel. We look forward to seeing you in Philadelphia.
ABOUT THE MEDTECH CONFERENCE
Featuring world-class plenary speakers, a wide array of educational programming,
valuable networking and business development opportunities, The MedTech
Conference is a must-attend event for the industry’s prominent and most promising
companies. The 2018 MedTech Conference presents 125 exhibitors and 3,000
attendees from 40 states and 30 different countries.
ABOUT China Med Device, LLC
China Med Device, LLC (https://ChinaMedDevice.com) provides turn-key solutions
for western medical device/IVD companies to enter China with regulation and
commercialization services. Our CFDA regulatory services cover strategy, RA, clinical
evaluation, CRO, QA and post market compliance. We are experienced in handling
innovation approvals and priority reviews. Our commercial services cover market
assessment research, reimbursement, partnership, distribution qualification and
management. We have offices in Beijing, Suzhou and Boston. Our management
team has 100+ years of combined experience in medical device and IVD and has
been involved with 1,000+ CFDA certificates and 250+ companies’ success.
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