Irina Golovacheva

Biography

Dr. Irina Golovacheva oversees the regulatory process from the initial study submission and receiving an approval up until end of study notifications for each project conducted by GCT in Russia. Irina is located in Moscow, within easy reach to the Ministry of Health and other agencies. Her responsibilities comprise of filing necessary applications, ensuring control of all Sponsor’s study documents to be submitted to the state regulatory bodies, and further – handling all interactions with MoH, Rosdravnadzor (Federal Service for Surveillance in Healthcare) and other authorities. Irina dedicates a fair share of her time for research to stay on the cutting edge with changes in the clinical trials regulations, combining it with regular participation in industry trainings and official seminars on the same topic. These facts, put together with her critical thinking ability and detail-oriented approach assure 100% successful regulatory track record for GCT and our Sponsors.  

Research Interest

Dr. Irina Golovacheva oversees the regulatory process from the initial study submission and receiving an approval up until end of study notifications for each project conducted by GCT in Russia. Irina is located in Moscow, within easy reach to the Ministry of Health and other agencies. Her responsibilities comprise of filing necessary applications, ensuring control of all Sponsor’s study documents to be submitted to the state regulatory bodies, and further – handling all interactions with MoH, Rosdravnadzor (Federal Service for Surveillance in Healthcare) and other authorities. Irina dedicates a fair share of her time for research to stay on the cutting edge with changes in the clinical trials regulations, combining it with regular participation in industry trainings and official seminars on the same topic. These facts, put together with her critical thinking ability and detail-oriented approach assure 100% successful regulatory track record for GCT and our Sponsors.