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Pre-clinical and Clinical Trials
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Pre-clinical and Clinical Trials
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Capio Diagnostik a.s in Copenhagen is GLP certified, ISO 17025 accredited, GCP compliant and has been FDA audited.
The laboratory serves the pharmaceutical industry and the biotech industry with:
- Method development
- Method transfer
- Method validation
- PK-sample analyses
- Bio-analytical Reports
- Central laboratory services
- Central logistics
Special strength in the following techniques:
- ELISA
- RIA
- Molecular biology
- Metal analyses
For further information please contact:
Yvonne Lech, Managing Director.:
Tel.: +45 3374 3091 Mobile: +45 2344 1284 Fax: +45 3374 3030 E-mail: yvonne.lech@capio.dk
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