You need to understand your process, define what the acceptance criteria is, and then challenge the process. The idea is once you have a validated process, you don’t have to look at the acceptance criterion each time, just monitor that the process is under control.
Monitor process while performed under controlled conditions
Define successful results beforehand
Challenge the process
Determine efficient ways to monitor the successful process
Document the process testing
Hello, good people of the world! So you have a cGMP warehouse you need to qualify? Well, this post will provide plenty of information to get you started.
First, how do you know your warehouse is a “cGMP” warehouse. Well, it is if:
Any examples of common or even possible non-cGMP warehouse space in the Biopharma industry? Please leave a comment below.
So what do you do? I hope you already have a SOP to handle these. If not, let me get you started!
Welcome back good people of the world! If you’ve been in “the industry” long, you’ve surely run across ISPE and maybe you’re even a member. I’ve been a member most of my career but don’t have any other strong affiliation, and feel like I talk about the group in an unbiased way. Continue reading The ISPE Guides – How Useful Are They?
Welcome good people of the world! Whether you’re an Engineer at a pharmaceutical company, a Quality representative in Biotech, or just someone interested in learning a bit more, you are making the world a better place.
Commissioning, Qualification, Verification, Validation – what does it all mean?
This blog contains FREE INFORMATION – always and forever.
I have over 10 years of validation experience, and am here to share what I’ve learned and to learn from you – please comment!
What topics would you like to see posted?
Mike Williamson Validation 