We ensure your suppliers meet the highest pharmaceutical quality and compliance standards. Our Supplier Qualification Audits identify, assess, and continuously monitor vendors to strengthen your quality supply chain.
We begin by collecting supplier data and evaluating historical performance to define risk levels and audit scope based on product criticality.
Our experts coordinate with your team to design an audit plan that covers objectives, timelines, and documentation requirements.
Auditors evaluate manufacturing practices, documentation, and systems at the supplier site to ensure compliance with GMP standards.
We identify non-conformities, deviations, or weaknesses in quality systems and provide practical recommendations for improvement.
Our detailed audit report highlights base on fact findings, risk levels, and corrective actions, promoting transparent communication with the supplier.
we extensively monitor the CAPA plans proposed by the supplier and ensure timely closure of the CAPA plans.
Upon successful CAPA verification, we finalize and archive the audit report in accordance with your QMS documentation standards.
We help identify and mitigate weak links in your supply chain through continuous supplier assessment, risk-based classification, and proactive quality monitoring — ensuring uninterrupted operations and regulatory compliance.