FSI «SID & GP» is holding a training workshop with international participation for pharmaceutical inspectors
From 12 to 14 February, 2019, the State Institute of Drugs and Good Practices together with the FEDEGARI and the NoDeviation companies will hold a training workshop for pharmaceutical inspectors.
The main topics of the workshop to be held will be as follows:
- An overview of the key principles of the ICH Q12 guideline (Drug Product Lifecycle Management);
- Modern approaches to process validation with application of the QbD (Quality by Design), Continuous Process Verification and Ongoing Process Verification principles;
- Industrial methods of thermal sterilization: equipment and sterilization process validation;
- Current methods of industrial decontamination in pharmaceutical manufacture;
- Sterility assurance criteria.
The goal of the workshop is to present the most advanced knowledge and experience possessed by the designers and manufacturers of state-of-the-art pharmaceutical equipment (FEDEGARI) directly supported by international experts in pharmaceutical quality management (NoDeviation) to pharmaceutical inspectors.
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”