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ABS Laboratories has considerable experience in the conduct of clinical bioanalytical packages for inclusion in drug marketing authority applications (MAAs) submitted to regulatory and licensing bodies.

Services offered include:

  • Custom assay development and validation.
  • Assay transfer.
  • Support to first time in man studies (FTM) with agreed fast turnaround of data.
  • Support to Phase I – IV including proof of concept (PoC) and bioequivalence studies.
  • Non-compartmental PK analysis.
  • Short time from study end to report.
  • Flexible reporting to meet the client’s specific requirements.

For any queries on the scope of the services provided please contact the business development team through the Quick Quotation link.