About the Good Control Laboratory Practices COP
The GCLP COP has more than 750 members representing various industry fields such as R&D and production
among non-regulated mediums, regulated markets, students, and the pharmaceutical community. The GCLP COP
addresses issues related to the impact of laboratory processes on other areas of pharmaceutical
- Provide a forum for members to discuss issues of common interest in the area of GCLP with the primary
objective being to find solutions to common industry problems
- Pro-actively advocate the importance of GCLP amongst members and pharmaceutical industry
- Share best practices in the area of GCLP amongst ISPE members and constituents
- Create a vast body of knowledge in the area of GCLP that is easily accessible by ISPE’s GCLP COP
How to Get Involved
As a GCLP COP member you can access
technical discussions or download presentations or files.
You can complete a volunteer profile and share your expertise
with the community. Note that only ISPE Members can engage in these activities.
method transfer activity validation
Good Control Laboratory Practices, 2 February,
Can anyone provide guideline on analytical method transfer from one site to other site wh ...
skip impurity testing in finished dosage forms
Good Control Laboratory Practices, 17 September,
During some documentation review I found out that a company skipped testing for impurities during re ...
Common microbiology incubator room?
Good Control Laboratory Practices, 6 March,
Can anyone advise whether it is advisable to have incubators for classical microbiology (where you w ...
Weighing Uncertainty / Minimum Weight
Good Control Laboratory Practices, 4 December,
Having completed the USP Section 41 "uncertainty" / minimum weight determination on all of our analy ...
Frequency of verification/ revalidation of analytical methods
Good Control Laboratory Practices, 30 October,
If a method has been validated or is a valid pharmapoeial method verified in a lab, what should be t ...