Qualtech is delighted to announce the upcoming webinar of our Southeast Asia Medical Device Compliance Update Series 2025, focusing on Singapore, Malaysia & the Philippines. This webinar is designed for medical device manufacturers, regulatory affairs professionals, and industry stakeholders seeking to strengthen their market access and compliance strategies in three of ASEAN's most dynamic healthcare markets.
Following the success of Part 1, which covered Indonesia, Thailand & Vietnam, this session will provide up-to-date insights, best practices, and practical guidance to navigate the evolving regulatory frameworks of Singapore, Malaysia & the Philippines effectively. These markets reflect Southeast Asia's dynamic and rapidly maturing medical device regulatory landscape, offering opportunities for both new entrants and established players.
Key Discussion Points
✦ Learn about the latest regulatory updates in Singapore, Malaysia, and the Philippines
✦ Understand how to navigate changing requirements and compliance challenges
✦ Get practical, experience-based insights from our local regulatory experts
Webinar Details
- • Date: Thursday, November 27, 2025
- • Time: 5:00 PM (GMT+8) | 10:00 AM (CET)
- • Language: English
- • Speakers: Qualtech's Local Regulatory Experts
- • Registration form: https://forms.gle/mZ61SAS1V5rQ4Kn16
This webinar will provide participants with insights to navigate the evolving regulatory environments of Singapore, Malaysia, and the Philippines with confidence.
Whether you are entering these markets for the first time or optimizing your existing compliance strategies, this session will equip you with the practical knowledge needed to stay ahead.
We warmly invite all interested professionals to join us for this informative session!
For any inquiries, please contact us at globalra@qualtechs.com
