The Global Bioequivalence Harmonization Initiative: Summary report for EUFEPS international conference

Eur J Pharm Sci. 2018 Jan 1;111:153-157. doi: 10.1016/j.ejps.2017.09.047. Epub 2017 Sep 28.


Bioequivalence (BE) is considered one of the key questions in new and generic drug product development and registration worldwide. However, the regulations and jurisdiction vary from country to country and continent to continent. Harmonization of regulatory requirements and criteria for BE determination may avoid unnecessary repetition of BE studies and minimize drug exposure to humans. Harmonization around the globe may be achieved by a better understanding of scientific principles and expectations from different regulatory authorities. To facilitate global harmonization, the Network on Bioavailability and Biopharmaceutics (BABP) under the European Federation for Pharmaceutical Sciences (EUFEPS) launched a Global Bioequivalence Harmonization Initiative (GBHI) several years ago. This international conference was the first in a series of workshops organized by EUFEPS/BABP under GBHI. The workshop provided a forum for pharmaceutical scientists from academia, industry and regulatory agencies to have open discussions on selected BE issues in the hope of identifying common ground and arriving at a harmonized view on these topics.

Keywords: Bioavailability; Bioequivalence; Biopharmaceutics; Global harmonization; Regulatory requirements; Regulatory standards.

Publication types

  • Review

MeSH terms

  • Congresses as Topic
  • Drug Approval / legislation & jurisprudence*
  • Drugs, Generic / pharmacokinetics
  • Excipients / chemistry
  • Government Regulation
  • Guidelines as Topic
  • International Cooperation
  • Pharmaceutical Preparations / chemistry*
  • Pharmaceutical Preparations / classification
  • Pharmacokinetics*
  • Therapeutic Equivalency
  • United States
  • United States Food and Drug Administration


  • Drugs, Generic
  • Excipients
  • Pharmaceutical Preparations