The experts at Inspired Pharma Training explain what a Quality Manual should contain and why it is important
A Quality Manual is a top-level document that describes an organisation’s Quality Management System (QMS). It is a document that was first required by the ISO 9001 standard for Quality Management Systems. It can be used both internally (for employees) and externally (for customers and auditors). It is common for a good auditor to ask to see a Quality Manual in advance of an audit to get a feel for the organisation’s QMS. By looking at the contents of a Quality Manual then an auditor will start to get an appreciation of an organisation in advance of an audit.
Chapter 4 of European Union Good Manufacturing Practice (EU GMP) covers the documents and records required by a pharmaceutical manufacturing site, yet unfortunately it makes no mention of a Quality Manual or what its contents should be. So is a Quality Manual needed to comply with GMP? Well the answer is yes. In Chapter 1 of EU GMP, covering the Pharmaceutical Quality System, it states “the Pharmaceutical Quality System should be defined and documented. A Quality Manual or equivalent documentation should be established and should contain a description of the Quality Management System including management responsibilities” (clause 1.7). So it is a requirement to have a Quality Manual, but we get little guidance of what it should contain, other than “a description of the Quality Management System including management responsibilities”.
Chapter 4 of EU GMP (Documentation) should give more detail of the contents of a Quality Manual, yet unfortunately this is missing. This is likely to be due to the fact that when Chapter 4 was last updated (June 2011) there was no mention of a Quality Manual in Chapter 1 at that time, which was then later updated in January 2013. Hopefully any future update of Chapter 4 will include more detail of what should be contained in a Quality Manual.
We can though turn to ICH Q10 (the Pharmaceutical Quality System) where additional guidance is also provided as to the contents of a Quality Manual. Clause 1.8 states:
A Quality Manual or equivalent documentation approach should be established and should contain the description of the pharmaceutical quality system. The description should include:
In other words the Quality Manual should contain
It is normal for a Quality Manual to be structured around the standard on which it is based, and so if a Quality Manual is based around the requirements of EU GMP, then it is normal to have a section of the Quality Manual corresponding to each of the nine chapters of EU GMP. Poor Quality Manuals normally involve simply copying the requirement of the standard into the manual itself. This is of little value. A good Quality Manual covers how an organisation intends to achieve the requirement of the standard that it is based on, for example:
A Quality Manual is a very useful document that not only gives guidance and direction to an organisation’s own personnel, but gives a potential customer, inspector or auditor an appreciation of an organisation from the outside. If designed well it can be used as a tool to sell an organisation, to show what a positive quality ethos they have and can show how good an organisation is and how seriously it takes its Quality Management System.