Clinical practice

What distinguishes accredited clinical photobiomodulation from unregulated consumer devices — and which clinics are listed as references.

Criteria for accreditation

Certified medical laser equipment with documented regulatory status (e.g. FDA 510(k)).
Practitioner training in neurology or adjacent medical disciplines, verifiable.
Documented, individualised treatment routines — never one-size-fits-all dosimetry.
No disease-cure claims; outcomes are always referenced to clinical studies.

Reference clinics

The institute maintains a third-party registry of clinics that meet the criteria above. Listing is descriptive and does not constitute a commercial endorsement.

View the registry of reference clinics →