Background
Yiting has over 17 years of experience in the medical technology field in industry and
government. Currently the Head of Regulatory Affairs for APAC at Alcon, Yiting is
responsible for developing and implementing regulatory strategies to support business
objectives and ensure compliance with local regulations across APAC markets.
Yiting is actively involved in regional harmonization work and was a member of various
Work Groups in AHWP and APACMed. In addition to his role as working member of
these harmonization groups, he is also a speaker in several editions of ASEAN Medical
Device Committee Meeting (AMDC) and AHWP Annual Training Workshops, with
topics ranging from Postmarket Surveillance, Pre-market Registration and Artificial
Intelligence Medical Devices. As a member of the APACMed RA Capacity Building
Committee and he has most recently worked with AHWP, APACMed & Deloitte in the
publishing of the Competency Framework for MedTech Regulators.
Since 2015, Yiting has been serving as an instructor for the Graduate Certificate in
Medical Device Regulatory Affairs (GCMDRA) by National University of Singapore,
covering topics from Pre to Postmarket as well as country regulations (US, EU, China,
ASEAN etc.)
Education
National University Singapore Jul 08-Dec 10
• Masters of Science (Materials Science and Engineering)
Nanyang Technological University Jul 03-Jun 07
• Bachelor of Engineering (Bioengineering) (2nd Upper Hons)
Certification
• RAPS Regulatory Affairs Certification (US)
• ISO 9001 Lead Auditor
• ISO 13485 Internal Auditor