Clinical Trial Support and Logistics - Project Support and Data Management
Proactive data managment
Eurofins Pharma Services built in collaboration with our clients an outstanding experience in data management. Our project managers start planning on data management just after the fist contact with the sponsor to define all project specifics:
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Key Personnel
- Investigator/Site details
- Patient Information
- Specimen Collection Supplies and Packaging
- Lab Results Report
- Electronic Data Transfer
- Website Access
- Sample Storage…
Specific instructions and control of data accuracy
Prior to the beginning of the study, specific instructions are created in the format of a laboratory manual or nurse manual. These specific instructions are applied on sample storage, processing of the samples and controls of demographic data. We have developed within Eurofins Pharma Services several procedures (programmed in SAS) to check the accuracy of the data. This coherence controls are applied prior to every data transfer and includes items such as number of parameters for each visit, missing data, crosscheck between center and patient number and accuracy of data encoding.
Customizable formats of reports
We provide complete customization of our reports which can save significantly time for our sponsors. Some examples of current report formats are:
- Monthly reports
- Intermediate data transfers
- Patient summary data report
- Patient inclusion report
- Kit delivery and expiry dates
- Kit use
- Logistic reports
We are used to edit special reports formats towards straight timelines. The increasing number of clients is a proof of our outstanding capacity in logistical support.
For further information please contact us: pharma@eurofins.com