Aseptic Excellence: 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
• Isolator/clean room decontamination with Hydrogen Peroxide

Breakfast and lunch will be provided, along with mid-morning and afternoon breaks.

Presented by:

Dr. Brian Bergin, Aseptic Technology & Design

Luisa Bernuzzi, Product and Applications Engineer at Mesa Labs

Host or Publisher Mesa Laboratories