Clinical governance is defined by the UK government for the NHS across the UK as:
A framework through which NHS organisations are accountable for continuously improving the quality of their services and safe-guarding high standards of care by creating an environment in which excellence in clinical care will flourish.
The NHS gained a statutory duty for quality of care in 1998 (see Health Act 1999).
Clinical governance can be thought of in terms of seven pillars:
- Service User/Patient Involvement.
- Clinical Audit and Quality Improvement.
- Staffing and Staff Management.
- Clinical Effectiveness.
- Risk Management and Safety.
- Data and Information.
- Education and Training.
In short, it's about doing the right thing, at the right time, by the right person—the application of the best evidence to a patient's problem, in the way the patient wishes, by an appropriately trained and resourced individual or team. This is essentially the aim of the Right Decision Service, so clinical governance sits at the heart of delivering RDS toolkits.
But this aim of clinical governance can only be fulfilled if it is underpinned by core values and ways of working within the organisation. Individuals and teams need to work within an organisation that is accountable for the actions of its staff, values its staff (appraises and develops them), minimises risks, and learns from good practice, and mistakes. These elements of clinical governance are all reflected in the quality checklist (Request form part 3) for RDS toolkits.