An overview of the key requirements for analysis of clinical trial samples.
This guide is ideal for laboratory staff, investigator site team members, sponsors, monitors, auditors and others involved in the analysis of clinical trial samples. The content is based on the European Medicines Agency’s “Reflection Paper for Laboratories that Perform the Analysis or Evaluation of Clinical Trial Samples” (2012) and the relevant principles of ICH GCP E6(R2).
e-book Good Clinical Practice for Laboratories
- Product Code: e-book Good Clinical Practice for Laboratories
- Availability: In Stock