Services

Clinical Trials

Specific coordinator for each study – site support for all lab samples related matters.
Participation in meetings withinvestigators
Organization of the collection and delivery of samples
Regulatory authorizations for samples importation/exportation
Design and supply of study sampling kits
Communication of the alert values
Adaptable and customizable reports of results according to each protocol needs
Sample storage (freezers -20 °C, -70 °C and liquid nitrogen)
Document archives according to CGP requirements
Electronic data transfer
Specific data base for each study
21 CFR Part 11 compliance