Medical Device Control Division, Food and Drug Administration (FDA,) has established a process to
offer consultation to educate researchers and medical device manufacturers, who are operating in
the research and development phase, and to provide information to support compliance to Medical
Device Act B.E. 2551 and its amendments, including other relevant laws. This will be useful in research
planning and medical device product registration in the future.
It is considered one of the main initiatives to help promote Thailand to become a comprehensive
medical hub, in preparation for transition into an aging society, to keep up with the rising health and
beauty trend, as well as to be ready for various epidemic situations in the future.
Interested researchers or medical device manufacturers may request consultation from the Medical
Device Control Division, by telephone at 02 590 7250 or at e-mail md_consultation@fda.moph.go.th
