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AI transcription consent form: Paragraph 25.4 rules

How to draft an AI transcription consent form for your Irish private clinic under Paragraph 25 of the Medical Council Guide. Access our template.

Ask Brigid Team
7 October 2026 · Updated 7 Oct 2026

Researched and written by Ask Brigid's AI pipeline and published automatically — not individually reviewed by a person. Useful as a starting point; check clinical, legal and regulatory details against a primary source before relying on them.

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Under Irish professional standards, patient confidentiality remains a cornerstone of private practice, but it is not absolute. The Medical Council Guide to Professional Conduct and Ethics (Effective 1 January 2024) outlines specific duties for registered practitioners regarding patient data. Paragraph 25 states that except where required by law or in the public interest, patient consent is required for the disclosure of information about them to others within or outside the healthcare team. For a private urologist operating across multiple sites—such as the Beacon, Blackrock Clinic, or the Mater Private—this obligation extends to every piece of documentation generated during a consultation, from a prostate-specific antigen (PSA) follow-up pathway to a complex flexible cystoscopy report. Furthermore, Paragraph 25.4 explicitly dictates that doctors must make sure that patient information in their control is protected against improper disclosure, access, or loss. When introducing digital tools that process voice or text, the responsibility for securing that information rests entirely with the consultant.

Why AI transcription requires explicit patient agreement

Using speech-to-text tools to document clinical findings is a standard administrative workflow. However, modern AI transcription differs fundamentally from traditional dictation systems. Instead of an encrypted local audio file sent directly to a medical secretary, AI transcription involves capturing raw audio of the live dialogue between doctor and patient, which is then processed by cloud-based servers to generate a written draft. Because a voice recording constitutes personal data, capturing the patient's voice alongside highly sensitive clinical details—such as symptoms of haematuria, erectile dysfunction, or prostate cancer staging—requires clear, documented authorization. To remain compliant with Paragraph 25.4, you cannot rely on implied consent. A dedicated patient consent form for recording must be completed before the consultation begins. This ensures the patient understands:
  • That their voice is being recorded during the consultation.
  • How the recording will be processed (for example, to generate clinical draft notes for clinician review).
  • Where the data is hosted and when the raw audio will be deleted.
For example, when using Brigid to record a consultation, the platform transcribes the audio and prepares a structured draft for the clinician to review, edit, and sign off. To support this workflow legally and professionally, an explicit voice recording consent form must be signed by the patient and filed in their electronic record. Consider a typical clinical scenario: Mr. O'Connor is attending your rooms for a benign prostatic hyperplasia (BPH) assessment and a review of his flow rate results. Before he enters the consulting room, your medical secretary presents him with the consent documentation. To ensure clarity, the form must be written in plain language. Below is a practical template designed for private specialist practices in Ireland.

Patient Consent Form for Voice Recording and Transcription

Practice Name: [Practice Name / Consultant Name]

Patient Name: ___________________________ DOB: _______________

We use secure, professional speech-to-text technology to assist in drafting your clinical notes and referral letters. This helps us maintain highly accurate medical records and reduces administrative delays.

Please read and sign the following agreement:

  1. I consent to the audio recording of my consultation with [Consultant Name] for the sole purpose of generating written medical notes and correspondence.
  2. I understand that the audio recording is processed securely in the European Union (AWS Dublin) and is deleted immediately after the written draft is finalized and saved to my medical record.
  3. I understand that the software does not make any clinical decisions, diagnoses, or treatment recommendations; all clinical decisions are made solely by my consultant.
  4. I understand that I can withdraw my consent at any time before or during the consultation, and this will not affect my care in any way.

Patient Signature: ___________________________ Date: _______________


Implementing a clear ai transcription consent form like this ensures that the patient is fully informed before any recording device is activated. It also establishes a clear audit trail, demonstrating that you have taken active steps to protect patient information from improper access or loss, as required by Paragraph 25.4.

Securing patient records under Paragraph 25.4 requirements

Once the patient signs the audio recording consent form, your administrative duties do not end. Paragraph 25.4 requires you to actively protect that information against loss or improper disclosure. This means you must evaluate where the data goes after the microphone is switched off. Many general-purpose AI transcription tools route data to servers outside the European Economic Area (EEA), which introduces significant professional and regulatory risks. For Irish private consultants, maintaining data within the EU is critical to aligning with clinical data standards in Ireland. When selecting software for your practice, verify the following security and storage parameters:
Requirement Standard for Irish Private Practices
Data Hosting Location Must be hosted within the EU (e.g., AWS Dublin region).
Encryption Data must be encrypted both in transit and at rest.
Audio Retention Policy Raw audio files should be deleted immediately after the transcription is verified and saved by the clinician. Only the finalized text record should remain.
Third-Party Sharing No clinical data or recordings should be used to train public AI models.
By enforcing these technical boundaries, you ensure that your use of transcription technology does not compromise the confidentiality central to the doctor-patient relationship. This is particularly vital when preparing sensitive clinical records, such as those required for medico-legal consultation dictation in Irish practices. To prevent administrative bottlenecks, your clinic needs a clear, repeatable process for managing consent without adding to your secretary's daily overhead. Here is a practical workflow for managing your ai transcription consent form process:
  1. Pre-Arrival Intake: Send the consent form to the patient before their appointment. Patients using the MyBrigid companion patient app can complete intake forms and sign consent documentation securely on their own phones before they ever set foot in your waiting room. This puts the patient in control of their own data sharing and eliminates paper-handling in the clinic.
  2. In-Clinic Verification: If the patient has not completed the digital form, your medical secretary should hand them a physical copy of the recording consent form template upon arrival.
  3. Filing and Archiving: Once signed, the consent form must be scanned and attached directly to the patient's electronic medical record. If using a digital platform, the signed consent should be linked to the specific consultation session.
  4. Consultation Check: Before starting the dictation, verify that the consent status is clearly visible on your screen. If the patient has declined, proceed with standard manual note-taking or traditional dictation workflows.
By establishing this routine, you protect your practice from professional liability while leveraging modern tools to manage waiting lists, clinic sessions, and multi-insurer billing across Vhi, Laya Healthcare, Irish Life Health, and Level Health. To begin implementing this workflow, review your current clinical intake forms and update them to include explicit language regarding voice recording and EU-based data processing.

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