Distribution of Medicines – Quality Management Systems (QMS)

The Good Distribution Practice of Medicinal Products for Human Use (2013/C 343/01), issued in November 2013, mandates that all distributors put into place a Quality Management System that outlines their processes for handling medicinal products.

Having a documented Quality Management System is fundamental to achieving a WDA (H). It needs to contain the firm’s Quality Policy, Management Dedication, Standard Operating Procedures, Risk Assessments, GAP Analysis and Training Records.

We can assess your business and help you to create a Quality System that is in line with the Guidance issued by the Medicines and Healthcare Products Regulatory Agency (MHRA) Inspectorate. This system will detail all necessary procedures and be compliant with MHRA standards

We can help you keep your quality management system up-to-date and adhering to the regulations

Why Consider Us for Quality Management Systems?

We are well-versed in developing and carrying out Quality Management Systems and can aid in the process at any phase. With a deep experience of making tailored Quality Management Systems for numerous clients, we have substantial expertise in both regulatory and business demands.

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For further details, please Contact Us