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.

Topics covered include:

  • 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

Running time: 24 minutes

Additional information

License Type

Single Use (Play on 1 Computer or use DVD Player and Monitor) ($310), Network/Plant Wide (WMV Files for Use on Shared Drive) (+$310.00)


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