Page 42 - 2018食藥署年報(英文版)
P. 42
Electronic Submission
& Online Application
Platform
Refuse-to-File
for Drug
Registration
Advancement
& Consultation
of Drug Review
System
Management of
Regenerative
Medicine
Advancement of
Pharmaceutical
Clinical Trial Review
System
Consultation
on Medicinal Products
APEC Regulatory Science Training Center of Excellence
TFDA Organized the “2017 APEC Good Registration Management (GRM)
Regulatory Science Center of Excellence Workshop.”
Policy on Management Establish Good Distri- Advancement of PIC/S
Orphan Drug Policy on Medicinal Drug Patent bution testing technolo- Meeting
Management Product Trace Linkage Practice gy on illegal
and Track System System (GDP) drugs