NHS England’s National Report to Ministers on the Responsible Officer Regulations and Medical Revalidation, 2016/17
In May 2017 all responsible officers were asked to complete the Annual Organisational Audit (AOA) for 2016/17 on behalf of their designated bodies. All 821 known designated bodies in England submitted a return, resulting in a 100% response rate. Collectively the results provide assurance to patients, the public, the service and the profession that the systems and processes underpinning revalidation are in place, and are working effectively, to ensure that every licensed doctor’s fitness to practise is monitored and assessed on a regular basis.
- NHS England’s National Report to Ministers on the Responsible Officer Regulations and Medical Revalidation, 2016/17
Framework of Quality Assurance for Responsible Officers and Revalidation (FQA)
The Framework of Quality Assurance for Responsible Officers and Revalidation (FQA) has been designed to assist responsible officers in providing assurance to their organisation’s board (or an equivalent governance or executive group) that the doctors working in their organisations remain up to date and fit to practise. The process, and collection of information it requires, supports responsible officers in the preparation of their own appraisal portfolios, giving an overview of their performance as responsible officers, whilst also providing a formal record of compliance, which will be helpful in the event of a designated body’s systems and processes becoming subject to challenge at any stage.
All responsible officers are asked to present an annual report (a template can be found at Annex D) to their Board or equivalent management team. Following this, a statement of compliance (with the regulations, template at Annex E) should then be signed off by the Chief Executive or Chairman (or executive if no board exists) of the designated body’s Board or management team and submitted to the higher-level responsible officer by 29 September 2017.
The purpose of the AOA exercise is to support designated bodies and responsible officers in providing assurance that robust systems and processes are in place, identifying areas in which development will be required over the coming year and engaging Boards and management teams in that endeavour.
Annex A – Core standards (of the Responsible Officer Regulations)
Annex B – Quarterly Report (for designated bodies to report their medical appraisal progress to their higher-level responsible officer).
The collection has been approved by the Burden Advice and Assessment Service (BAAS), formerly Review of Central Returns – ROCR, reference ROCR/OR/2236/001MAND
The BAAS team (formerly ROCR) are keen to receive feedback on central data collections from the colleagues who complete/submit returns. In particular, around the length of time data collections take to complete and any issues, suggested improvements or duplication of data collections. Feedback can be submitted to BAAS using the Data Collection Burden Reduction Service referral form.
An email containing a link to an electronic version of the form will be sent out during April 2017. The questionnaire should only be submitted using the electronic version. Please do not use the form available on this webpage for your submission.
Annex E – Statement of Compliance (for the chief executive or chairman, or executive if no board exists, to sign a statement of the organisation’s compliance to the Responsible Officer Regulations and submit to their higher-level responsible officer no later than 29 September 2017).
Annex F – Independent verification (a process by which all designated bodies will undergo to validate the status of their revalidation systems at least once in every 5-year revalidation cycle)
There is draft guidance and a specification available for those who wish to commission an external review.
Annex G – Bench-marking, calibration and checking consistency (the processes in place to enhance consistency across the country, in terms of approach, decision-making and thresholds for intervention)