Drug Supply Management


For each trial it is crucial that the investigational product is properly managed throughout its life cycle from release to destruction.
Our Study Drug Managers ensure that the IP has been manufactured and checked in accordance with internationally accepted standards of GMP for medicinal products for human use, track and guarantee the timely delivery of the IP at the investigational site(s) throughout the trial and assist the CRA and investigational site in all aspects of drug accountability.

Our services include:

Our Services