Eurofins in your country
At Eurofins Medinet, we pride ourselves on going the extra mile – routinely providing the added extras that you wouldn’t normally expect from a contract service organization.
Our study directors are able to fully manage any project and are pivotal in communicating between the various units of the project team.
Challenge us with your most demanding compound and discover that we deliver excellent de novo method development and validation, as well as cross validation and method transfer.
Available technologies running under GLP include (multi-component) LC-MS/MS, HPLC, GC-MS, immunochemistry, enzymatic assays as well as elemental analysis (ICP-AES).
Data integrity is of paramount importance and, by continually monitoring both data quality and our laboratory operations, we can ensure that the highest standards are maintained.
Size is not important. Our well-equipped laboratories and knowledgeable staff have the flexibility to handle both urgent, high volume, and smaller ‘one off’ projects.
Clients can rely on our experienced team of coordinators who take full responsibility for the logistics of every study.
All analytical data are captured and managed electronically in our Watson LIMS and safeguarded with electronic archiving (NuGenesis) and backup procedures compliant with regulatory requirements, in particular 21 CFR Part 11. The analytical data can be supplied in the format that best matches the client’s internal data management systems.
All final reports include a thorough review of laboratory data as well as reviews from the study director, laboratory facility management and independent QA staff, to support the integrity of your study data. All material can be customized to the clients’ specifications for convenience.
Eurofins in your country