The pharmaceutical industry is facing significant challenges with the current Annex 1 requirements: increasing regulatory expectations, growing complexity of aseptic processes, and the pressure to implement new production capacities quickly and in a compliant manner. Topics such as the protection of first air, the minimization of manual interventions, and containment require a fundamental shift in equipment and process design.

In this webinar, we demonstrate in a practical way how these challenges can be successfully addressed. The focus is on innovative technologies and integrated solution approaches that enable a safe, efficient, and future-proof implementation of Annex 1 requirements.

Using a fully integrated Aseptic Vial Processing Solution, we show how regulatory requirements can be consistently translated into an end-to-end equipment concept – from automation and hygienic design to containment and monitoring.

Experience an Annex 1-compliant overall solution that not only impresses technically but is also available in the near term – FAT-ready in 2027.

📢 Experts in the webinar

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