As part of the yearly update, this half-day seminar presents participants the opportunity to hear from regulatory certification experts.
The presenters will share the latest changes and updates for MedTech Regulatory Compliance including topics on Clinical Evaluation & Market Surveillance.
This seminar is organised by Singapore Institute of Manufacturing Technology (SIMTech).
Our expert, Ms Li Yang, Assistant Vice President, Chemical Centre of TÜV SÜD PSB is invited to speak on Regulatory Requirement for Biocompatibility Test on Medical devices.
11 March 2014 (Tuesday)
SIMTech Auditorium, Tower Block, Level 3
9.00am - 12.30pm ( Registration starts 8.30am )
Who Should Attend
This seminar is designed for a multidisciplinary audience of Directors, Managers, Department Heads, Supervisors, Senior Specialists from:
- Quality Control and Assurance
- Quality Management
- Quality by Design
- Regulatory Affairs
- Process Development
- Process Engineering
Registration for this seminar is free of charge and seats are available on first-come, first-served basis. To reserve a place, please click here.
For more details, please contact Mr John Lim Kee Yong, Senior Consultant, PE COI, Tel: 6793 8248, Email: kylim@SIMTech.a-star.edu.sg.