Our expertise
Euromedex is an experienced partner of the CROs and the promotors of clinical trials.
Euromedex takes in charge every aspect of the logistic of the clinical trial.
Whatever the regulatory status of the therapeutic units (narcotics, psychotropes, products of biologic
origin) or the temperature conditions of the product, Euromedex delivers a tailored service.
All the service provided is delivered in the strict respect of the regulatory constrains and the
reference tables GMP/GDP which are at the basis of the quality assurance system of Euromedex.
Our assets
Dedicated room : managed and controlled temperature
Skilled and polyglot collaborators
Customer service : high quality individualized contacts
Reactivity : Delivery in France at day D+1
Geographical situation : in the heart of Europe
Strict Quality Assurance : complies to pharmaceutical standarts
Treatment of the administrative formalities :
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
Logistic operations :
EUROMEDEX proposes its service of logistical centre and central pharmacy for all the logistical
operations : reception, control of the products, storage, delivery to the experimentation sites
(delivery at day D+1, in France), return of the non-used therapeutic units, reconciliation and control
of the quantities, destruction.
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 registrated in EUROMEDEX Data Base or in the IVRS System.
Managed temperatures :
According to the needs, the logistical operations can be performed at managed temperatures :
- 20°C, + 4°C, ambient temperature. Euromedex guarantees quality and security of
storage in dedicated rooms.
Additional performances :
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.
EUROMEDEX proceeds also to the pick-up and the return of the products from the investigation
centers. At the end of the study EUROMEDEX does the reconciliation of the products before
organizing their destruction or the return to the manufacturer.
EUROMEDEX can provide the comparator medicine, the medical devices and the material needed for
the performance of the clinical trials.
Supply of the medicine or medical device used as a comparator
Management and logistics of the documents and the randomization envelops
