Clinical studies with a view to safety
Every new drug is tested in clinical trials to investigate its safety and effectiveness. All products administered to participants must be produced according to Good Manufacturing Practices (GMP) and then distributed according to Good Distribution Practices (GDP). For the clinical trial itself, the Good Clinical Practices (GCP) obviously apply.
“Clinical Trial Supply Management is at the crossroads of GMP, GDP and GCP. Good management of the supplies - the experimental drug, but also any other product and necessary device - is crucial to ensure the continuity of the study and the safety of the participants.”Ilse – Associate Business Manager
Clinical Trial Supply Management – Advipro @ your service
- Operational support in Clinical Trial Supply Management
- Establishing and implementing supply processes