09/03/2026
New POPIA Health Regulations: What Every Practice Must Verify Before Releasing Patient Records
The Regulations relating to the Processing of Data Subjects’ Health Information by Certain Responsible Parties (2026) came into force on 6 March 2026.
They introduce new compliance duties for:
• Insurance companies
• Medical schemes
• Scheme administrators
• Managed care organisations
• Pension funds
• Certain employers
For clinicians, this changes how requests for patient records from these entities should be handled.
The starting point: Patient consent
Under POPIA, health information is special personal information.
The default position is simple:
Do not disclose patient records without consent.
Consent must be:
• Voluntary
• Specific and informed
• Given in writing
• Limited to the purpose disclosed to the patient
Obtaining consent remains the safest and most defensible basis for disclosure.
When these regulations apply
The 2026 regulations become relevant when these entities process health information without consent, relying on Section 32(1)(f) of POPIA (processing authorised by specific laws, regulations or collective agreements).
In those circumstances they must:
• Conduct a Legitimate Interest Assessment (LIA) documenting purpose, necessity and balancing of interests
• Rely on a specific legal basis — not general “administrative needs”
• Notify patients if information will be transferred outside South Africa
• Implement security safeguards and retention limits
What this means for your practice
Best practice remains to obtain patient consent for third-party disclosures, even when a requester asserts a legal basis.
However, you may sometimes receive requests where consent is unavailable or refused, and the requester relies on Section 32(1)(f).
You are not responsible for conducting their LIA. But you must ensure you do not facilitate unlawful processing.
Before releasing records without consent, verify:
• Their category — Do they fall within the regulated entities?
• Their legal basis — Can they identify the exact law, regulation or collective agreement authorising the processing?
• LIA compliance — Have they conducted the assessment? Request written confirmation.
• Cross-border transfers — Will records leave South Africa and has the patient been notified?
• Minimum necessary disclosure — Share only what is required and document what was released and under what authority.
Why this matters
The Information Regulator is actively enforcing POPIA.
If a disclosure is challenged, the key question will be:
“What steps did the practice take to verify that this request complied with POPIA and the 2026 regulations?”
Practices that prioritise consent — and verify carefully when consent is absent — build truly defensible practices.