Manufacture of Medicines for Clinical Trials
$310.00 – $620.00
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
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)