Regulatory obligations within the pharmaceutical supply chain are rapidly increasing, making quality management more complex than ever. As manufacturing expands into emerging markets and standards tighten worldwide, drug companies must ensure quality and compliance across their entire supply chain—a task that requires deep expertise and global reach.

The Kent Group is a trusted partner specializing in quality management systems audits and certifications, with a strong foundation in Good Manufacturing Practices (GMP). Our global network of independent auditors is experienced in US FDA and European Commission regulations, offering tailored solutions for pharmaceutical quality assurance.

We provide comprehensive cGMP and risk-based audit services for manufacturers, suppliers, and regulators, as well as consultancy, training, and gap analysis. Our expertise ensures consistent, reliable compliance monitoring and quality control, no matter where your operations are based.

With over 30 years of experience and a proven track record, The Kent Group delivers actionable insights and support for pharmaceutical and biotech supply chains—locally and globally.

Call 973.402.5888 today or contact us to learn more about our Pharmaceutical Quality Management Systems Audits and Certification services.