The QP needs an understanding of the microbiological control of pharmaceutical products.
Delegates will discuss the main types and sources of micro-organisms and the issues
associated with them in relation to sterile and non-sterile pharmaceutical production.
Specific sessions cover water systems, clean room design and operation, and the concept
of sterilisation and sterility assurance.
Delegates will discuss the main types and sources of micro-organisms and the issues
associated with them in relation to sterile and non-sterile pharmaceutical production.
Specific sessions cover water systems, clean room design and operation, and the concept
of sterilisation and sterility assurance.
