Annex 1 and First Air: Critical Considerations for Cleanroom Design and Compliance

Annex 1 and First Air: Critical Considerations for Cleanroom Design and Compliance

The implementation of EU GMP Annex 1 marks a transformative shift for the sterile filling industry. With new requirements emphasizing barrier technology and “first air” contamination control, pharmaceutical manufacturers face critical decisions in adapting their processes. Johannes Rauschnabel of Syntegon explores how equipment suppliers can play a pivotal role in facilitating compliance and seamless integration of these advanced standards.