In the biomanufacturing world, a huge diversification of products takes place with new therapeutic approaches emerging. Join Sartorius Stedim Biotech in November for a training course on Single-Use Bioprocessing in GMP-regulated environments.

Sartorius Stedim Biotech Ltd will be hosting a new training course on Single-Use Bioprocessing in GMP-regulated environments. The course will be offered by the Parenteral Drug Association (PDA) Europe in cooperation with Sartorius Stedim Biotech on the 26th and 27th of November 2019 with an optional third day on the 28th. 

Upon completion of the course, participants can expect to have understood the regulations and relevant guidelines for single-use system (SUS) handling, explain basics in single-use processing operations including the use of bags, tubings, filters and sensors.

Participants will also understand Data Integrity and Data Analysis / Monitoring for SUS handling and possible setups for filter and container closure integrity testing in single-use assemblies.