Aseptic manufacturing for pharmaceutical and biopharmaceutical products is being regulated and standardized as this practice continues to grow in the industry. With the publication of EU Annex 1 in Europe, there are strict guidelines to assure compliance of the aseptic process.
Join us for a full-day seminar presenting valuable information regarding the control of aseptic processing to meet cGMP requirements.
What you will learn:
- Overview of aseptic processing
- Steam sterilization of product, containers and/or devices
- Biological indicator selection and services to validate and monitor your processes.
- Isolator/clean room decontamination with Hydrogen Peroxide
Breakfast and lunch will be provided, along with mid-morning and afternoon breaks.
Dr. Brian Bergin, Aseptic Technology & Design
Dr. Andreas Demmler, Optima
Luisa Bernuzzi, Product and Applications Engineer at Mesa Labs
Date and time
Thursday, March 14 · 8:30am - 5pm CET
Hilton Vienna Park