Guidelines for Industrial Data Integrity are Published
The State Institute of Drugs and Good Practices in cooperation with PQE Group has come up with a draft of Guidelines for Data Integrity and validation of computerized systems in pharmaceutical industry. The draft is available at the Institute’s website. Please follow the link to familiarize with it; your feedback is appreciated. The authors welcome questions and comments at: dataintegrity@gilsinp.ru
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”
