Qualification and validation of sterile and single-use filtration systems remain key challenges for pharmaceutical and biotechnology manufacturers. This is a topic on which we are regularly consulted, particularly in the context of ongoing supply chain challenges and the growing need for reliable backup solutions.

On September 24 in Brussels, Pemflow is hosting a dedicated workshop focused on practical approaches to the qualification and validation of sterile and single-use filtration systems.

During this workshop, we will share practical recommendations based on field experience and discuss the key considerations involved in qualifying filtration systems. We will also be joined by our partner laboratory LPP, whose expertise in filtration validation and upcoming regulatory developments will bring valuable insight to the discussions.

The event will provide an opportunity to exchange on your own applications, discuss practical cases and ask questions directly to specialists involved in qualification and validation projects.