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GCP (Good Clinical Practice) is an international standard of ethical and scientific quality for conducting a clinical trial on drugs involving humans. GCP includes all aspects of a clinical trial, i.e. from the time the trial is planned and conducted until the results of the trial are reported.
The purpose of GCP is to ensure that the rights, safety, and well-being of test subjects are protected and that clinical trial data are credible, as described in the Declaration of Helsinki. Following the GCP ensures that the data collected are valid, complete and well documented.