We provide GMP compliance consulting, pharmaceutical quality audits, Quality Management System (QMS) advisory, vendor and supplier qualification, regulatory inspection readiness, CAPA and investigation support, and technical and validation advisory.

We support organizations across the pharmaceutical and allied healthcare sectors, including pharmaceutical manufacturing, API manufacturing, formulations, contract manufacturing, contract testing labs, the pharmaceutical supply chain, and healthcare and allied industries.

Our approach is designed to provide objective assessment, practical recommendations and sustainable quality improvement. We understand your processes, assess against GMP requirements, identify gaps and risks, recommend practical actions, support improvement, and verify the effectiveness of what was implemented.

No. While MS GMP and Quality Advisory has strong expertise and extensive experience in the pharmaceutical industry, our consultancy services are not limited to this sector. We also extend our support to organizations across various industries seeking to establish, implement, maintain, and improve their Quality Management Systems (QMS) in accordance with ISO 9001:2015 requirements. Our services include QMS gap assessment, documentation development, implementation support, internal audit, management review guidance, and preparation for ISO certification audits. We are committed to helping organizations strengthen their quality systems, improve operational effectiveness, and achieve continual improvement.