OVERVIEW OF ORPHAN DRUG DESIGNATION (ODD) PROCESS IN JAPAN
GRP’s presentation provides an overview of the Orphan Drug Designation (ODD) Process in Japan.
March 25, 2021
Manufacturing Sites Accreditations in Japan
GRP’s presentation outlines important information on Manufacturing Sites Accreditations in Japan.
February 15, 2021
Regulation of Regenerative Medicine in Japan
GRP’s presentation outlines important information on regulations concerning regenerative medicine in Japan.
February 15, 2021
Real World Data in Japan
GRP’s presentation outlines important information on approaching real world data (RWD) in Japan.
February 15, 2021
Drug Master File (DMF) in Japan
GRP’s presentation provides an overview of Drug Master File (DFM) Registration in Japan.
June 9, 2020
Global Regulatory Partners GK: Current Capabilities in Japan
GRP’s presentation provides an overview Global Regulatory Partners capabilities in Japan for in country representation Medical Device registration, Foreign Manufacturing Site Accreditation (FMA) and Reimbursement.
May 19, 2020