Bioequivalence is an essential scientific standard for ensuring that medicines are safe, effective, and therapeutically reliable. Its mastery not only ensures quality in treatments but also strengthens professional practice in clinical, regulatory, and research areas.

This course, offered by CECYPE in partnership with Simulations Plus, provides comprehensive training ranging from physiological and pharmacokinetic fundamentals to report interpretation and the practical application of bioequivalence in clinical and pharmaceutical development settings.

It is designed for:

• Professionals in pharmaceutical development, bioanalysis, regulation, and clinical research.
• Researchers in clinical pharmacology, pharmacokinetics, biostatistics and bioanalytical validation.
• Graduate students in pharmaceutical sciences, biotechnology, chemistry and related fields.
• Health officials, regulators and consultants.
• Staff from CROs, pharmaceutical laboratories and clinical study managers.
• Teachers, trainers, and leaders seeking to integrate an applied and updated vision of bioequivalence.

Participants will acquire the necessary skills to interpret, apply, and communicate bioequivalence with scientific rigor, strengthening its impact on professional practice, regulation, and innovation in medicine.