To promote the exchange of information and cooperation in areas pertinent to medical products and the relevant administrative and regulatory matters, The Central Drugs Standard Control Organization (CDSCO) of the Republic of India under the Ministry of Health and Family Welfare and the Ministry of Health, Labour and Welfare of Japan (MHLW) concluded the Memorandum of Cooperation (MOC) in 2015.
Based on this MOC, PMDA co-holds symposia with CDSCO regularly and organizes some seminars for CDSCO.
Bilateral Arrangements
Memorandum of Cooperation (December 2015)
Symposia
The India-Japan Symposium is planned and co-hosted by CDSCO and PMDA to tighten the mutual relationship and the cooperative framework for regulation of medical products and to promote thorough understanding of regulatory systems of the two host countries. The latest three symposia are shown here.
7th
Date: July 10, 2024
Location: New Delhi, India
Number of participants (Approx.): 100
Program and Materials
6th
Date: February 1, 2023
Location: Online
Number of participants (Approx.): 380
Program and Materials
5th
Date: December 21 to 22, 2021
Location: Online
Number of participants (Approx.): 300
Program and Materials
Seminar
PMDA organizes the seminar for CDSCO based on their requests.
FY 2023
Regenerative Medicinal Products Review
Date: June 28, 2023
Location: Online
Number of participants: 30
Report
Good Manufacturing Practice (GMP)
Date: May 29, 2023
Location: New Delhi, India
Number of participants: 80
Report
FY 2022
Good Registration Management (GRM)
Date: June 22, 2022
Location: Online
Number of participants: 40
Report
FY 2021
Regenerative Medicinal Products Review
Date: June 3, 2021
Location: Online
Number of participants: 39
Report
For other seminars, please click the Seminar Schedule page.