About this Event
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
- Rooms & RABS
- Isolator/clean room decontamination with Hydrogen Peroxide
Breakfast and lunch will be provided, along with mid-morning and afternoon breaks.
Presented by:
Luisa Bernuzzi, Product and Applications Engineer at Mesa Labs
Bruno Aze, VHP Global Senior Manager at Steris
Event Venue & Nearby Stays
Courtyard Arlington Crystal City/Reagan National Airport, 2899 Richmond Highway, Arlington, United States
USD 500.00
