Sinova Pharma is an independent UK-based pharmaceutical quality and regulatory consultancy delivering strategic regulatory advisory, GMP audit, inspection readiness, and Qualified Person (QP) certification services across UK and EU markets, enabling organisations to maintain compliance and deliver safe healthcare products to patients.

We work with Marketing Authorisation Holders, pharmaceutical & biotech companies, CDMOs, and importers to strengthen quality systems, manage regulatory risk, and remain inspection-ready under global GMP requirements.

Our approach is independent, risk-based, and commercially aware, safeguarding regulatory integrity while supporting operational continuity.