Representatives of FSI «SID & GP» of Minpromtorg of Russia took part in the workshop dedicated to automation of the pharmaceutical industry
On 08 November, representatives of the State Institute of Drugs and Good Practices took part in the workshop dedicated to automation of the pharmaceutical industry organized by the Ministry of Industry and Trade of the Russian Federation. The workshop saw speeches of experts representing leading manufacturers and suppliers of manufacturing systems and equipment for the pharmaceutical industry. A welcoming address was delivered by the Director of the Department of Pharmaceutical and Medical Industry Development of Minpromtorg of Russia Mr. Alexey Alekhin and the Director of FSI «SID & GP» Mr. Vladislav Shestakov.
Today, the modern pharmaceutical manufacture is placing exacting demands on product quality. At the same time, the interest of manufacturers with the priority to reduce production costs cannot be disregarded.
«Automation of processes allows to minimize process-related risks, to remove the human factor for the most part and, consequently, to secure high product quality,» said the Director of the Department of Pharmaceutical and Medical Industry Development of Minpromtorg of Russia Mr. Alexey Alekhin. «It is important to implement systems allowing for improvement of production performance, which will have an impact both on the competitive ability of the industry on the whole and on the competitive ability of products supplied not only to the Russian market, but exported abroad as well.»
The workshop saw speeches of experts representing Russian and foreign companies supplying equipment and manufacturing systems for pharmaceutical, biotech, chemical, and food industries. The experts shared with workshop participants their experience and best practices in automation of manufacture. The Head of Good Engineering Practices Department of FSI «SID & GP» Mr. Igor Falkovskiy highlighted the topicality of finished dosage forms manufacture following the up-to-date standards from the GMP point of view.
«Automation processes and explosive development of robotics technology are the reality which has become ingrained in our everyday lives. An in this regard, the pharmaceutical industry is one of the leaders,» said the Director of FSI «SID & GP» Mr. Vladislav Shestakov. «Here, the most innovative solutions have always been applied. Today, state-of-the-art technologies in the industry are on the front burner. We witness the growth potential and market interest in development of automation. Being an inspection authority, our Institute has exclusive expertise providing us with an opportunity to analyze the dynamics of development of the current manufacture of all types of dosage forms, including the most modern ones, as well as changes in the needs of manufacturers.»
- The Cooperation Agreement was signed between State Institute of Drugs and Good Practices and National agency of pharmaceutical products of Algeria
- SID&GP passed the recertification audit of the Quality Management System according to ISO 9001:2015
- Russian Federation has submitted an application for the Pharmaceutical Inspection Co-operation Scheme PIC/S accession
- SID&GP experts participated in the ISPE Eurasian Affiliate pre-conference
- Signing of Cooperation agreement between FSI “SID&GP” and Agency for medicinal products and medical devices of Bosnia and Herzegovina