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Our associate CROs are providing bioequivalence services to fulfil registration dossier requirements. We are providing complete package from protocol to final Report (with chromatograms). Our partner CROs are approved from WHO, USFDA, EU and DCGI.

Bioequivalence Studies

Φ As per EUCTD / USFDA/ DCGI guideline

Φ As per non-regulated mareket / semi-regulated guideline

Zodiac Advantage for Bioequivalence Services:

Φ Coordination for BE studies (on behalf of formulation manufacture)

Φ Low cost due to our long-term alliance with CROs

Φ Providing complete protocol, report and chromatograms

Φ Handling all pre-registration and post-registration queries

Bioequivalence studies format: As per country specific guideline.

For BE price quote or information, please write email to us: - info@zodiacpharma.com