Aseptic Excellence: A Mesa Labs & Steris Microbiological Validation Seminar

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

Host or Publisher Mesa Laboratories