Clinical Trial Support and Logistics - Drug Management

Logistic for Clinical Trial

Our activity is to provide logistics for clinical trials according to the specific needs of the Sponsor: from  preclinical  Clinical studies (phases I to IV) and postmarketing steps.

The performed studies are always carried out by professionals with a deep knowledge of pharmaceutical (GDP, GMP), shipment regulations and state of the art equipment.

Manufacturing

Our abilities and our agreements for importation of products for clinical trials enable us to propose you some services such as: batch release, secondary packaging and labelling.

Storage

Our facilities are equipped with large capacities of climatic rooms in controlled conditions (+20°C, +5°C, -20°C & -80°C). These installations are of course subject to qualification once a year.

Monitoring for storage conditions includes continuous recording of temperature, with the use of a 21-CFR Part-11-validated software.

Distribution

One of our main forces is our reactivity for delivery within 24/72 hours in Europe by some specialized courier companies.

Shipment packagings are always validated: i.e controlled temperature and follow-up of temperature.

Other services such as return from investigator sites and destruction of experimental drugs may as well be offered by us.

For further information please contact us: pharma@eurofins.com