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Prove the bioavailability/bioequivalence of your drug candidate with fast, accurate, cost-effective BA/BE clinical trials from SGS.

Clinical Research

Proving the bioavailability/bioequivalence of a drug candidate with reliable data, on-time and on budget, is a cornerstone for generic companies. With biological drugs now making up a large proportion of new drugs, this poses new challenges to generic companies as their “biosimilars” cannot be seen as true generics. 

Why choose bioavailability/bioequivalence clinical trials from SGS?

We provide you with:

  • A highly beneficial regulatory environment in Belgium, enabling a fast study start within two to three weeks from dossier submission to first subject screened
  • In-depth understanding of EC/CA local requirements and specificities
  • An 88-bed clinical pharmacology unit capacity
  • Bioanalytical laboratories for parallel samples dosing
  • Highly experienced biostatistics and PK groups to design studies and analyse data

With over 35 years of experience in early clinical trials, and unmatched Phase 1 expertise, we have the resources and facilities to deliver your bioavailability/bioequivalence clinical trials quickly and accurately.

Contact us today to discuss how we can help with your bioavailability/bioequivalence and biosimilar clinical trials.

This service is not currently available in this country. However, we have an unrivalled global network. Please contact us to discuss the delivery of this service.