ENSURING GLOBAL PHARMA COMPLIANCE FROM LAB TO LAUNCH
ENSURING GLOBAL PHARMA COMPLIANCE FROM LAB TO LAUNCH
Embedded Files
📞 Connect with iViTAA CONSULTANCY
IVITAA CONSULTANCY empowers pharmaceutical manufacturers, CROs, and laboratories with high-impact regulatory, GMP, and quality solutions — from system development to successful inspection outcomes.Â
Expert Pharma Compliance Partner
IVITAA CONSULTANCY is a regulatory and quality consulting firm based in Ahmedabad, India, led by highly rich experience persons, as a trusted partner to pharmaceutical companies in India as well Overseas , Our services are grounded in over 6 years of experience across Oral dosage form , NDDS Products ,Sterile, Nutraceuticals , API, Cosmatic and Biotech domains. We specialize in GMP compliance, Audit readiness, Regulatory Dossier Preparation ,Submission , Bioequivalence Report review and on-site Quality /GMP support.
Whether if you're navigating Local FDA,WHO, EMA or PIC/S inspections — we ensure for support to meet the highest international standards.
20+
20+
YEARS RICH EXPERIENCE
4+
4+
GLOBAL AGENCIES TIE UP
150+
150+
DOSSIERS & CLINICAL STUDIESÂ SUPPORTED
Comprehensive Services Across the Product LifecycleÂ
Trusted by Pharma Companies in India and OverseasÂ
We assist pharmaceutical & nutraceuticals manufacturers, CDMOs, Analytical labs, and API suppliers across ASEAN, LATAM, GCC, AFRICA, and Asia. Our insight into international regulations ensures your systems are audit-ready — every time.Â
Have a Compliance Challenge?
Let’s Solve It — Together.
All consultations are strictly confidential and handled by senior regulatory expertsÂ
Page updated
Google Sites
Report abuse