Center Specialists Participate in an International Seminar in Japan

Specialists from the Pharmacology Committee of the State Institution "Center for Pharmaceutical Product Safety" are actively participating in the "Multiregional Clinical Trials/Good Clinical Practice (GCP) Inspection Seminar - 2025" (MRCT/GCP Inspection Seminar 2025) organized by the Asia Training Center for Pharmaceuticals and Medical Devices Regulatory Affairs under Japanʻs Pharmaceuticals and Medical Devices Agency (PMDA-ATC).

The seminar aims to further develop inspection practices for pharmaceutical product development and clinical trials in accordance with international standards. During the event, participants have the opportunity to study advanced practices in multiregional clinical trials, discuss the requirements of GCP inspections, and attend masterclasses on their implementation.

This international seminar is being conducted by leading specialists from Japan and international experts. The event holds significant importance in enhancing the knowledge and skills of representatives from the pharmaceutical sector of our country, strengthening global partnerships, and introducing new practices aligned with international standards into local operations.