During the webinar we will present the basic requirements, expectations and challenges related to the implementation of an integrated system for modeling, validating and monitoring technological processes of manufacturing medicinal products, active substances and dietary supplements based on the QbD approach and real-time release of the product RTRT. The system is a response to changes introduced in the regulations of Good Manufacturing Practice.
The webinar is addressed both to research and development department employees interested in implementing QbD (Quality by Design) approach to quality assurance departments, who want to monitor the process in real time with the detection of unusual trends, and to technological departments that deal with increasing the efficiency of manufacturing processes of medicinal products.
