Friday 19 September 2008

Standards: Incidents, Problems and CAPA

An analysis of FDA Warning Letters issued over the past few years shows some recurring themes (see previous posts). One of these that consistently stands out is the regulations cited more than any other; 21CFR Part 820.100 Corrective and Preventive Action closely followed by 21CFR 820.198 Complaint Files.

In this blog I want to highlight what CAPA is, and also place it in the context in terms of Incident Management and Problem Management, alongside Complaints.

Incident Management and Problem Management

ITIL has a clear explanation of Incident and Problem Management and the difference between them. It goes like this; consider the following analogy:

Every city has a stretch of road where accidents seem to occur on a regular basis; so called “accident black-spots”. When an accident happens, the police are usually the first on the scene, quickly followed by other emergency vehicles as required: ambulances, fire, tow truck, etc. The first order of business is to attend to the injured. Next is to get the traffic moving again.

This is the essence of Incident Management; it is reactive and looks for an immediate, short-term solution.

Somewhere, people are gathering information and analysing that accident, what may have caused it and how it may relate to other accidents which occurred along that same stretch of road. They analyse, among other things, traffic patterns, the time of day, weather conditions at the time, road signage. From this analysis, they seek to determine the ROOT CAUSE of the accidents and thus find a means of preventing accidents.

This is the essence of Problem Management; it is proactive and looks for a permanent solution to prevent further incidents.

Corrective and Preventive Action

FDA Guidance says the following;

Corrective action is a reactive tool for system improvement to ensure that significant problems do not recur.

and...

Being proactive is an essential tool in quality systems management. Succession planning, training, capturing institutional knowledge, and planning for personnel, policy, and process changes are preventive actions that will help ensure that potential problems and root causes are identified, possible consequences assessed, and appropriate actions considered.

So the focus in these activities is to find root causes and ways to stop problems happening in the future, rather than righting what has happened in the past.

It is important to understand that CAPA is not an Incident Management process - CAPA is all about Problem Management; it is the same as ITIL Problem Management, with both reactive (triggered by incidents/failures) and proactive (triggered by other sources) activities.

The Incident Management process is essentially addressed by the "Complaint Files" regulation for medical devices (and others focussing on manufacturing incidents and adverse events). Perhaps this is a source for the large volume of citations for violation of these regulations; companies lack an understanding of the interface between Complaints (incidents) and CAPA (problems), which is much easier to understand when viewed from the ITIL framework.

GAMP Honorable Mention

As a footnote to this, it is worth mentioning that GAMP4 did not really address either incident or problem management. This has been corrected in GAMP5 with the addition of the Operational Appendices O4 Incident Management and O5 Corrective and Preventive Action. Note how GAMP employs language recognisable to IT stakeholders (incidents) and regulatory stakeholders (CAPA), bridging the gap of understanding that may have existed before.

No comments: