EUROMEDEX is an experienced partner of the CROs and the promotors of clinical trials.

All the services provided are delivered in the strict respect of pharmaceutical standards.

EUROMEDEX proposes its service of logistical center and central pharmacy for all the logistical operations:

reception, control and storage of products (dedicated rooms with controlled temperature: -20°C; +4°C; 15-25°C);

quick delivery to experimentation sites (delivery at day D+1 in France) with controlled temperature during transport;

at the end of the study, pick-up and return of non-used therapeutic units from investigation centers;

reconciliation and control of the quantities before organizing destruction or the return to the manufacturer.

For every medicine or each medical device, EUROMEDEX can take in charge :

the customs formalities for the importation or exportation of therapeutic units;

the pharmaceutical responsibility of all the logistics operations made for the clinical trials.

EUROMEDEX follows precisely and rigorously each therapeutic unit, document or associated material. The collected datas are available in real time for the organizer of the clinical trials.

Shipment and movement in stock are registered in EUROMEDEX Data Base or in the IVRS System.

In the frame of the organization of a clinical trial EUROMEDEX can offer following additional services :

EUROMEDEX can organize packaging or labeling operations for the therapeutic units, with adaptation of the texts and the languages in the respect of GMP in collaboration with other service providers.

Due to its international wholesaler status, EUROMEDEX can also provide the comparator medicine, the medical devices and the material needed for the performance of the clinical trials in addition to the management and logistics of the documents and the randomization envelopes.