Drug Substance Synthesis



Topics covered in this program include:

  • Where does GMP begin in R & D?
  • How does GMP in R & D, differ to GMP as it applies to the manufacture of medicinal products for sale?
  • The rationale of documentation as a means of providing a system of information and control
  • Process controls
  • Contamination control
  • Process controls
  • Explanation of the terms Validation and Qualification

Running time: 28 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) (+$465.00)


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