Bioequivalence Studies

Bioequivalence Studies

We offer bioequivalence study services through locally and internationally accredited research centers, ensuring that the generic drug has the same efficacy and bioavailability as the original product.

Category:

Bioequivalence Studies

The service includes:

  • Coordination with licensed centers (FDA, EMA, SFDA)

  • Scientific protocol design

  • Study execution and result analysis

  • Preparation of technical reports for regulatory submission

Benefit:
Ensures that generic drugs meet international standards in terms of quality and efficacy, which is a key requirement for their registration and market approval

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