To promote the regulatory convergence and enhance the efficiency and quality of the registration of the medicinal products among Asia-Pacific region, Taiwan Food and Drug Administration (TFDA) is hosting the ‘2023 APEC Good Registration Management (GRM) Center of Excellence (CoE) Workshop’ from September 6th to September 8th. TFDA has invited 20 experts from overseas and local regulatory authorities, the pharmaceutical industries and the academia to provide trainings for trainees.