A*STAR – HSA Regulatory Symposium

The symposium was jointly organized by A*STAR and Health Sciences Authority (HSA) with the aim to provide awareness and address the questions and concerns from the scientific, clinical and start-up/ SME community regarding the medical device regulatory framework and requirements in regional and international countries. It also covers common regulatory challenges faced in the industry and possible ways to address them.

This symposium was also for regulators, clinicians and engineers in the medical device industry for networking purposes.  In addition to the symposium, the organisers arranged one-to-one sessions for consultants to advice participants who are involved in medical device development.  The one-to-one sessions were for both parties to have the opportunity to look at the regulatory strategy for the device from the participants and explore a possible collaboration.

DH RegSys participated in the symposium with Ms Tan Hwee Ee as a speaker in the symposium. Her speech covered the regulatory outline of medical devices for US and EU. DH RegSys also participated in the one-to-one consultation session.