GV17270004
MANUFACTURE OF MEDICINES FOR CLINICAL TRIALS
The concept of GMP in an R & D environment. The difference between producing medicinal products for sale and producing development products for clinical trials. Regulatory Authorities and site inspections. Documentation in R & D, its significance and purpose. Contamination control. Cleaning and cleaning validation. How clean is 'clean'? The principles of Validation and Qualification.
DVD
24 minutes
USD 310.00
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