Come gestire una richiesta di accesso ai dati (SAR)
A clear guide to managing patient data requests lawfully and efficiently in general practice
Autore Thomas Andrew Porteus, MBCSPubblicato originariamente 9 Lug 2025
Rispetta le linee guida editoriali
- ScaricaScarica
- Condividi
- Language
- Discussione
- Versione audio
- Aggiungi alle fonti preferite su Google
Professionisti Medici
Gli articoli di riferimento professionale sono progettati per essere utilizzati dai professionisti della salute. Sono scritti da medici del Regno Unito e basati su prove di ricerca, linee guida del Regno Unito ed europee. Potresti trovare uno dei nostri articoli sulla salute più utile.
Subject access requests (SARs) are a legal right under the UK General Data Protection Regulation (UK GDPR), allowing individuals to ask for a copy of their personal data. In general practice, these requests most often come from patients - but can also be made by solicitors, third-party agencies, or even staff. Handled well, a SAR is an opportunity to demonstrate transparency and trust. Handled poorly, it can lead to delays, complaints, or even regulatory action. This guide walks you through the key steps to managing SARs confidently and compliantly, while staying on the right side of the law - and your patients.
What is a subject access request?
A subject access request is any request made by an individual for access to the personal data your organisation holds about them. In general practice, this could include:
Medical records.
Correspondence about the patient.
Consultation notes.
Test results or referrals.
Staff notes recorded about the patient.
Under the law, you have one calendar month to respond to a SAR, and you cannot charge a fee, unless the request is manifestly unfounded or excessive.
Who can make a SAR?
The patient themselves.
A parent or guardian (for children, depending on age and capacity).
A third party with the patient’s written consent (for example, solicitor, insurance company).
You must always verify the identity and legal authority of the requester. This may involve requesting ID and consent documentation.
How to respond to a SAR - step by step
1. Acknowledge and log the request
Log the date the request was received and who submitted it. Note the one-month deadline - this includes weekends and holidays. You should also:
Assign a responsible person to manage the request.
Use a standard SAR log or template (many ICBs provide one).
Add it to your practice’s IG calendar or risk tracker.
If you need more information from the requester to proceed (for example, clarify date range or consent), the one-month clock pauses until you receive it.
2. Confirm identity and consent
Ask for photo ID if the requester is unknown to you.
If it’s a third party (solicitor, insurer), ask for signed consent from the patient.
Ensure the consent clearly states what information may be shared and with whom.
If the request is made by a parent, check the child’s age and ability to understand. You may need to assess Gillick competence.
3. Gather the relevant records
Collect only the data that falls within the scope of the request. This might involve:
Searching EMIS, SystmOne, or your clinical system.
Extracting correspondence (for example, hospital letters).
Printing or exporting clinical notes.
Redacting third-party information (see below).
Avoid sharing:
Notes about other individuals (including staff).
Confidential third-party information.
Data not relevant to the patient.
Information that could cause serious harm.
If unsure, consult your Caldicott Guardian or Data Protection Officer (DPO).
4. Redact carefully and review
Before sharing the records:
Redact any third-party information, unless consent has been obtained.
Ensure safeguarding or risk information is appropriately considered.
Check for abusive or threatening language (which may need redaction or context).
You should document your redaction process in case of future challenge.
5. Send securely and confirm receipt
Provide the response in the patient’s preferred format, where possible. This could be:
Printed and collected in person (with ID check).
Posted securely via recorded delivery.
Sent electronically through a secure system or encrypted email.
Provide a cover letter outlining what is included and who to contact with questions.
6. Close the request
Once completed, record:
The date the SAR was fulfilled.
Who reviewed and approved it.
Any exemptions or redactions applied.
How the data was shared.
Keep this log securely - it may be needed for audit or complaint resolution.
Common pitfalls - and how to avoid them
Pitfall | Come evitarlo |
Missing the deadline | Log and calendar every request from day one |
Sending too much information | Define the scope clearly before you start |
Forgetting redactions | Always review before sharing |
Misidentifying the requester | Verify ID and consent for third parties |
Using insecure delivery methods | Encrypt or use secure post |
What if the request is complex?
If the SAR involves particularly large amounts of data, or you need more time to locate and review it, you can extend the deadline by a further two months - but you must notify the requester within the first month, explaining why.
Where to get help
Your DPO or ICB Information Governance lead.
NHS England guidance on subject access.
ICO SAR guidance: ico.org.uk.
Local CSU or IT support for redaction tools.
Final word: make it routine, not rushed
Subject access requests don’t need to be a panic-inducing chore. With clear templates, strong processes, and a shared understanding across the team, they become a manageable - and even helpful - part of your practice’s data responsibilities. Patients have a right to see their records. You have a right to respond in a way that protects privacy, safety, and trust.
Aggiornamenti esclusivi per i professionisti sanitari
Rimani informato con gli ultimi aggiornamenti clinici, approfondimenti professionali e linee guida basate su evidenze. La newsletter Patient Pro seleziona contenuti essenziali per i professionisti sanitari—consegnati direttamente nella tua casella di posta.
Abbonandoti accetti i nostri Informativa sulla Privacy. Puoi annullare l'iscrizione in qualsiasi momento. Non vendiamo mai i tuoi dati.
Informazioni sull'autoreVisualizza il profilo completo

Thomas Andrew Porteus, MBCS
SaluteTech
MBCS
Thomas scrive per informare, ispirare e attrezzare i leader delle pratiche e i professionisti della salute che affrontano il cambiamento, attingendo a due decenni di lavoro pratico nel sistema sanitario del Regno Unito.
Storia dell'articolo
Le informazioni su questa pagina sono scritte e revisionate da clinici qualificati.
Articolo disponibile anche in Inglese, Tedesco, Spagnolo, Francese, Italiano, Portoghese, Hindi, Ebraico, Arabo, and Svedese.
Prossima revisione prevista: 9 Lug 2028
9 Lug 2025 | Pubblicato originariamente
Autore:
Thomas Andrew Porteus, MBCS

Chiedi, condividi, connettiti.
Esplora le discussioni, fai domande e condividi esperienze su centinaia di argomenti di salute.

Non ti senti bene?
Valuta i tuoi sintomi online gratuitamente
Più su governance e sicurezza delle informazioni
- Legge sull'Uso e l'Accesso ai Dati 2025 - cosa significa per la pratica generale
- Come evitare mal di testa IG quando si lavora con il personale PCN
- Come condurre una valutazione del rischio IG a livello di pratica
- Come creare una cultura di consapevolezza IG nella tua pratica
- Come creare un calendario IG pratico che funzioni davvero
- Come gestire una violazione dei dati dei pazienti
- Come gestire le domande comuni dei pazienti sulla sicurezza delle informazioni
- Come gestire la sicurezza informatica in un ambiente di lavoro ibrido
- Come prepararsi per una presentazione DSPT senza panico
- Come prevenire la condivisione delle smartcard e perché è importante
- Come rispondere a un'email sospetta in meno di 60 secondi
- Come condurre un aggiornamento IG di 15 minuti alla tua prossima riunione di team
- Come individuare e fermare i rischi IG interni
- Come formare il personale sulla sicurezza informatica senza annoiarlo
- Come scrivere un'informativa sulla privacy per i pazienti che ispira fiducia