Conducting a joint training GMP-inspection
On June 4 and 5, 2018, at the production site of solid dosage forms (Istanbul, Turkey), employees of FSI “SID & GP” – Vladimir Orlov, Deputy Head of the department of scientific and methodological work and training, and Vitaly Kazyulkin, Chief specialist of the department for inspection of medicines production, conducted a joint training GMP inspection with representatives of the regulatory entities of the Republic of Kazakhstan and the Kyrgyz Republic. This event was a continuation of the educational activity of the institute within the framework of the GLO project (Global Learning Opportunities) in cooperation with the World Health Organization.
The main goal of the training inspection was the exchange of experience between the regulatory entities of the EAEU member states in the field of inspecting of pharmaceutical production facilities for compliance with the requirements of the rules of good manufacturing practice of the EAEU, the formation of the common inspection principles, as well as the further development of interregulatory dialogue in view of the expected launch of GMP-inspection procedures within the Union.
Other materials
- FSI “SID & GP” and CDSCO, India signed a cooperation agreement.
- The importance of reference samples in the development of pharmaceutical industry was discussed during the meeting of the Healthcare Commission of the General Council of the UNITED RUSSIA Party
- The program of the IX All-Russian GMP Conference with international participation has been published
- Attendees of the ‘Ensuring Drug Security’ Forum discussed issues of public trust in the Russian pharmaceutical products
- Vladislav Shestakov took part in the 8th International Pharmaceutical Congress Russia – Nicaragua “Evolution of Production Potential: Localization of Production to Strengthen the International Health Care System”
