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Consent forms: templates and legal obligations

Published on March 29, 2026 · 9 min read

Informed consent is a cornerstone of the therapeutic relationship. In Switzerland, it is both an ethical obligation and a legal requirement. With the entry into force of the nLPD in September 2023, consent requirements for the processing of health data have been significantly strengthened.

This guide covers the two types of consent needed in a therapy practice, the mandatory elements of each form, and best practices for efficient management.

Disclaimer: this article is provided for informational purposes and does not constitute legal advice. Consult a lawyer or your professional association for analysis tailored to your situation. Requirements vary by canton (cantonal health laws).

Art. 321 CP — Professional secrecy: alongside the nLPD, art. 321 of the Criminal Code protects therapists’ professional secrecy. Sharing clinical information beyond billing data requires explicit patient consent, under penalty of criminal sanctions.

The two types of consent

As a therapist, you need two distinct consents:

1. Consent to therapeutic treatment

Based on Swiss medical law and the Code of Obligations. The patient must be informed of the nature of the treatment, risks, alternatives and costs before giving their agreement.

2. Consent to personal data processing

Required by the nLPD (RS 235.1) for the processing of health data (sensitive data). Must be explicit, informed and freely given.

Informed consent to treatment

Informed consent to treatment must cover:

  • Nature of treatment: describe the proposed therapy in understandable terms
  • Objectives: what the treatment aims to improve
  • Risks and side effects: even minor ones (skin reactions, soreness, etc.)
  • Alternatives: other possible therapeutic approaches
  • Duration and frequency: expected number of sessions, duration of each session
  • Costs: rate per session, insurance coverage
  • Right of withdrawal: the patient can stop the treatment at any time

Consent to data processing (nLPD)

According to art. 6 para. 7 nLPD, consent for the processing of sensitive data (including health data) must be explicit. Your form must indicate:

  • Which data: identity, contact details, date of birth, medical history, session notes, invoices
  • Why: therapeutic follow-up, billing, communication
  • Who has access: yourself, your management software, insurers (via the invoice)
  • Where data is stored: server location (Switzerland ideally)
  • How long: retention period (10 years minimum for medical records)
  • Patient rights: access, rectification, deletion, portability
  • Withdrawal of consent: clear and simple procedure

Paper vs digital

Swiss law does not require a specific form for consent. Both formats are valid:

CriteriaPaperDigital
Legal validityYes (handwritten signature)Yes (timestamp + checkbox)
ArchivingPhysical folderAutomatic, encrypted
SearchManualInstant
SecurityRisk of physical lossEncryption + backup
UpdatesNew form to signRe-consent in one click

Recommendation: digital consent is more practical, more secure and easier to manage daily. It must nonetheless include a timestamp, the connection IP and an active confirmation (checkbox, not pre-checked).

Common mistakes

Implicit consentassuming the patient consents simply by attending the session. The nLPD requires explicit consent for health data.

Single merged formmixing treatment consent and data consent. If possible, separate them clearly so each is understandable.

Overly legal languagea form the patient doesn’t understand is not “informed” consent. Use simple and clear language.

No withdrawal procedurethe patient must be able to withdraw their consent easily. Document the procedure.

Non-archivingnot keeping proof of consent. In case of dispute, this is your primary protection.

Best practices

  • Present the form before the first session, not during
  • Take the time to explain each point — it’s a moment of trust
  • Offer a copy to the patient (email or paper)
  • Update your forms at least once a year
  • Keep proof of consent for the entire duration of follow-up + 10 years
  • Document any withdrawal of consent with the date and consequences explained

Digital consent in Therago

Therago integrates a nLPD-compliant digital consent system: customisable pre-configured form, electronic signature with timestamp, automatic encrypted archiving, and one-click withdrawal procedure. Each consent is linked to the patient file and can be consulted at any time.

Manage your consents in full compliance with Therago.

Free 30-day trial

No credit card required. Data hosted in Switzerland.

Consent forms: templates and legal obligations | Therago