Webinar
Digitize with Precision: Mastering Carry Over Calculations in Cleaning Validation
Transform cleaning validation from an afterthought to a streamlined, digital process that ensures compliance and minimizes risks!
Cleaning validation is often treated as an afterthought in pharmaceutical manufacturing, but with every new guidance released cleaning validation has over time changed from a simple verification that equipment has been cleaned to a robust program to ensure that cleaning procedures reduce and minimize product impact from residues and cleaning agents.
In this webinar, we will explore how we traditionally utilize residual limit or carryover calculations to ensure the cleanliness of our equipment and the types of challenges we face utilizing manual or disparate tools. We will also touch on the consequences of cleaning processes designed without proper carryover calculations in mind.
Afterwards, we’ll look at how we can tackle some of these challenges in Process Manager and how we can leverage a robust digital system to ensure that our carryover calculations meet the quality requirements that are expected of us in the current pharmaceutical world.