Location & Organised by: BioTech Training Facility
Growth promotion testing, environmental monitoring, sterility testing, bioburden and endotoxin testing. What do the results really mean?
And: How are these methods executed and validated?
What does a microbiological “Out of Specification” mean for the production process?
Participants of this course are going to answer these questions using a mix of theory and practical training.
After completion of this course the participants will be able to place microbiological results correctly within the context of GMP and patient safety.
Please register via www.biotechtrainingfacility.com