On June 22, the PMDA held the “PMDA-ATC Good Registration Management (GRM) Webinar 2022 for CDSCO”. This webinar was designed for staff members of the Central Drugs Standard Control Organization (CDSCO), India, who are engaged in review of pharmaceuticals. A total of 40 CDSCO regulators was participated in it.
The PMDA and CDSCO exchanged their views regarding the importance of pre-application consultation as well as the acceptance of overseas clinical trials in line with post-marketing requirements.
The PMDA continues to promote collaboration with CDSCO through training seminars and other activities etc.
See attached program