In accordance with GCP guidelines clinical trials materials and Investigational Medicinal Products that have been: used, partially used, unused or expired must be accounted for and disposed in an appropriate manner. During and upon completion of the clinical trial process, IMP CSS will handle all required services concerning returns, reconciliation and destruction in accordance with GMP/ GCP regulations and local regulations. Our dedicated personnel liaise the returns with the investigational sites, account for and store the returned items in a dedicated area. Upon client’s approval, the performed destruction will follow with a destruction certificate.

We aim to provide immaculate service to our wide range of clientele: CRO, start-ups, international pharmaceutical companies and more.

You can depend on our expertise to provide all clinical supply management tailor-made for your clinical trial.