Experts in Pharmaceuticals discussed "How to become an authorized person on pharmacological control? Introduction of the pharmacological control system in production" at the seminar held at the "State Center for Expertise and Standardization of Medicines, Medical Products, and Medical Equipment."  

At the event, the head of the Association of Representative Offices of Foreign Pharmaceutical Companies and Manufacturers, Muhabbat Akbarova, general director of the National Pharmacological Research Center, RQA, member of the ISOP Association Anatoly Krasheninnikov and head of the Pharmacological Control Department of the State Center Elvira Svechnikova, as well as employees of the Pharmacological Committee of the State Center, about 40 representatives of foreign pharmaceutical companies and manufacturers participated.

At the beginning of the seminar, Elvira Svechnikova, the head of the Department of Pharmacological Control, explained what pharmacy control is. She noted the primary purpose of the pharmacy control system, their summary of normative documents on pharmacy control in the Republic of Uzbekistan, prospects for the development of the pharmacy control system, and the implementation of the pharmacy control system by manufacturers. In addition, she provided information on the principles of performance, the pharmaco-control system's components, and the pharmaco-control system's documents.

After that, Anatoly Krasheninnikov, Doctor of Pharmaceutical Sciences, reported on the regulatory requirements for the pharmacy control system, the role of the authorized person in pharmacy control in the organizational structure of the company, the duties of the authorized person in pharmacy control, and the obligations of the authorized person in pharmacy control.

The participants' questions, including about 50 participants connected through the "Zoom" platform, were answered during the event.

State Center Information Service