Regenerative medicine

It may only be prescribed by doctors, dentists or podiatrists with the appropriate qualifications and experience, using suitable equipment or instrumentation, and in duly authorised healthcare facilities and centres.
Professionals may only perform the functions within their own area of specialisation, and staff training is essential to justify the appropriate use of PRP technology.

It is the prescriber's responsibility to select the PRP system most appropriate for the specific pathology being treated. That system must have demonstrated efficacy for that pathology. The prescriber is also responsible for ensuring the quality of the system, even if processing and preparation are carried out by a third party.

No. To ensure efficacy, safety and reproducibility of clinical outcomes, the system requires the exclusive use of BTI centrifuges. These feature a pre-set acceleration and braking programme that is essential for preparing the final product and achieving the desired clinical outcomes.

Yes. PRGF-ENDORET® holds all certifications required by international health authorities (including CE marking and approval by medicines regulatory agencies). In addition, the system strictly complies with the quality and reproducibility criteria required for classification as a non-industrially manufactured medicinal product for human use.

The single-use kits include ALL the materials required to prepare the final product, from collection through to activation.

Yes. The use of PRGF-ENDORET® technology requires prior training. This ensures that clinical staff have precise knowledge of the preparation protocol, thereby ensuring reproducibility of results and compliance with current health regulations.

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