Meeting EU GMP Annex 1 and PUPSIT Requirements for Fill Finish Processes with Single-Use Systems

WEBINAR

As drug manufacturing regulation such as EU GMP Annex 1 continues to evolve, so does the manufacturing equipment to help ensure the highest levels of the safety and sterility of medicinal products for human use. Single-use systems can enable you to meet these regulatory needs, such as PUPSIT, while tailoring them to fit your fill finish process requirements.

In this webinar, you will learn how you can implement PUPSIT with manual operation or fully automated to minimize risks in sterile filtration processes and how next generation, gloveless isolators with single-use filling assemblies are simplifying your contamination control strategy (CCS).

In this webinar, you will learn:

• How to interpret the EU GMP Annex 1 regulation
• What this regulation means for your fill finish process and equipment
• Industry trends such as fully automated PUPSIT systems and gloveless isolators using single-use systems