PK Reports for Bioequivalence Studies in just 24 Hours from Concentration Data Upload

Press Release – Clinical Research Services Turku CRST
PK Reports for Bioequivalence Studies in just 24 Hours from Concentration Data Upload

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Contact Supplier: Clinical Research Services Turku CRST
Supplier Press Release: PK Reports for Bioequivalence Studies in just 24 Hours from Concentration Data Upload
Address: University of Turku – CRST, FI – 20014 University of Turku, Finland
Tel: +358 2333 7502, +358 2333 7635
Fax: +358 2251 0046
Website: www.crst.fi

12 JULY 2012

PK Reports for Bioequivalence Studies in just 24 Hours from Concentration Data Upload

CRST’s bioequivalence package offers PK reports for bioequivalence studies in just 24 hours from concentration data upload. Bioequivalence testing of drug products is conducted in compliance with Good Clinical Practice and EMA’s Guideline on the Investigation of Bioequivalence. BE studies are conducted effortlessly with competitive pricing with CRST’s full-service trial package:

• Clinical study protocol and report writing
• Regulatory submissions
• eCRF
• Clinical conduct with efficient recruitment of healthy volunteers
• Study monitoring
• Project management
• Analysis of PK samples in our in-house GLP-accredited bio-analytical laboratory
• Data management in collaboration with our partner StatFinn Ltd.
• PK calculations and statistical analysis by StatFinn Ltd. with eBESTbio, a cloud reporting tool to create a PK report in just 24 hours from the concentration data upload.

For more information or to discuss bioequivalence studies please contact us directly.

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