We provide end-to-end support including Global Dossier Filing, eCTD Publishing & Submission, Quality (cGMP & GxP) Audits, and US Agent & FDA Registration to help you meet global compliance standards.
Get StartedOur expertise includes Pharmacovigilance, Toxicology Assessment, Medical & Scientific Writing, and EU / UK MAH & QP Services to ensure your products remain compliant and market-ready worldwide.
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VAAH Global Regulatory & Quality Solutions is a trusted regulatory consulting and services company dedicated to supporting life sciences and healthcare organizations across the entire product lifecycle. We provide end-to-end regulatory, quality, safety, and compliance solutions that enable our clients to navigate complex global regulatory landscapes with confidence.
To be a globally recognized regulatory solutions partner, delivering excellence, integrity, and innovation across the life sciences and healthcare ecosystem.
To empower life sciences organizations with reliable regulatory solutions that ensure compliance, protect patient safety, and accelerate global market access.
Medical Writing and Technical Writing are specialized disciplines that transform complex
Quality, GMP, and GxP Audits are essential for ensuring compliance with regulatory requirements
eCTD, CTD, ACTD Publishing and Submission is a standardized electronic
We operate as an extension of our clients’ teams, providing strategic guidance and operational support tailored to specific regulatory, technical, and business needs.
We are here to bridge the gap between rapid innovation and stringent regulatory frameworks. We assist organizations in:
VAAH Global Regulatory Solutions was founded with a clear vision: to simplify regulatory complexity while maintaining the highest standards of quality, integrity, and scientific excellence.
086-6884-6495
info@vaahsolutions.com
www.vaahsolutions.com
Hyderabad, Telangana, India - 500081