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Registration Number: {{org_field_registration_no}}


DC25-Notification of Other Incidents Policy

1. Purpose

The purpose of this policy is to establish a clear and structured approach for the notification, reporting, and management of incidents that may impact service users, staff, visitors, and the overall operation of {{org_field_name}}. Ensuring timely and accurate reporting allows for appropriate investigations, risk mitigation, and regulatory compliance with the Care Quality Commission (CQC), Health and Safety Executive (HSE), and local authorities.

This policy implements the statutory notification duties in the Care Quality Commission (Registration) Regulations 2009 — Regulations 16 (deaths), 17 (MHA-related), 18 (other incidents) and 22A (form of notifications) — and the Duty of Candour (Regulation 20). It also embeds RIDDOR 2013 reporting to the HSE, UK GDPR breach reporting to the ICO, outbreak escalation to UKHSA and safeguarding duties under the Care Act 2014 (adults) and Working Together to Safeguard Children (2023) (where applicable).

By implementing this policy, we aim to foster a culture of transparency, accountability, and continuous improvement, ensuring that all reportable incidents are addressed effectively and preventatively.

2. Scope

This policy applies to:

It covers:

3. Legal and Regulatory Framework

This policy aligns with the following legal and regulatory requirements:

4. Definition of Reportable Incidents

Incidents that must be reported include but are not limited to:

Incidents requiring CQC notification under Regulation 18

Mental Capacity and DoLS (adults)

Medicines and Medical Devices

Report suspected adverse drug reactions or medical device incidents via the MHRA Yellow Card scheme; also follow local clinical governance routes.

5. Notification and Reporting Procedures

To ensure immediate action and regulatory compliance, all incidents must be:

Duty of Candour (Regulation 20) – what we do when harm meets the threshold

When an incident meets the notifiable safety incident threshold, we tell the person/family as soon as reasonably practicable, offer an apology, provide written follow-up, and keep a record of all steps taken. (The overarching duty to be open and transparent applies in all cases.)

6. Investigation and Follow-Up Procedures

Each incident undergoes a structured investigation process to ensure root causes are identified and preventive actions are taken. The investigation follows these steps:

7. Corrective Actions and Risk Prevention

To prevent recurrence of incidents, corrective actions may include:

Share learning and track it (de-identified) through team meetings and the risk register; cross-reference to the CQC Single Assessment Framework quality statements for Safe and Well-led.

8. Compliance Monitoring and Continuous Improvement

To maintain high safety standards and regulatory compliance, {{org_field_name}}:

9. Policy Review and Updates

This policy is reviewed annually or sooner if:

This policy will be reviewed immediately following changes to CQC notification guidance/portal, RIDDOR reporting instructions, UKHSA outbreak guidance, or ICO breach-reporting rules, and at least annually thereafter.


Responsible Person: {{org_field_registered_manager_first_name}} {{org_field_registered_manager_last_name}}
Reviewed on:
{{last_update_date}}
Next Review Date:
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Copyright © {{current_year}} – {{org_field_name}}. All rights reserved.

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