We treat every record as a patient safety matter.
Pruvance Quality Systems Private Limited is a global life sciences consulting and professional services company.
Compliance for Patient Safety.
We support pharma, biotech, life sciences and CDMO organizations in maintaining inspection readiness. Pruvance delivers 21 CFR Part 11 compliant QMS documentation across Deviation, CAPA, Change Control, Complaints, SOP Management and Training, as well as Regulatory Affairs, Pharmacovigilance and PMO support.
We combine scientific expertise, regulatory understanding and practical industry experience to help you strengthen quality systems, address resource gaps and advance critical projects efficiently.
Specialist support across the life sciences lifecycle.
Five principles behind every engagement.
Compliance
Regulatory requirements drive how each document is built and reviewed.
Data integrity
Accurate, complete and traceable records from draft to approval.
Scientific excellence
Technical depth so documents stand up to expert scrutiny.
Security
Controlled handling of your confidential material.
Partnership
Long-term collaboration with your quality and regulatory teams.
From first call to inspection-ready.
Discovery call
We listen to your situation, your inspection history and the regulations that apply to you.
Scope and plan
You receive a clear scope, timeline and team, with deliverables defined before work begins.
Deliver and review
Our specialists deliver, your team reviews, and independent checks confirm quality and data integrity.