GMP audit and inspections for pharmaceutical industry suppliers and subcontractors remain a critical part of the drug development and manufacturing process. An experienced GMP auditor who can evaluate and monitor supply chain stakeholders, can drive greater insight which enables you to improve control over quality.
All regulatory agencies who set standards for the pharmaceutical industry have an expectation of Good Manufacturing Practice compliance, for example, across production supply chains. As a consequence, you will have an obligation to engage with your increasingly complex supply chain, and all supply chain actors including a multitude of suppliers, service providers and subcontractors.
Our team of senior GMP auditors have in depth experience of conducting pharma audits to GMP, knowledge of the pharmaceutical regulatory standards, expectations and procedures. We conduct regulatory GxP audits in the pharmaceutical industry against the applicable regulatory texts or standards such as Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and Good Laboratory Practice (GLP).
Why work with LSQA Middle East?
We offer comprehensive GMP auditing and certification solutions to manufacturers around the world. Utilizing our global network of specialists, we will support you in implementing and verifying GMP compliant processes that demonstrate your commitment to supplying products to global markets.
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