PhysioSense extracts structured data from systematic reviews and guidelines — every value traceable to PMID, page, and quoted text. Built by clinicians, for everyday practice.
Specialist in Applied Physiotherapy in Neurorehabilitation with 12 years of clinical experience. Graduated top of class from the University of Montenegro, Faculty of Medicine — Applied Physiotherapy program. Currently completing Master's studies in the same field.
Built PhysioSense to solve the problem he faced daily: evidence from studies exists, but reaching it takes longer than seeing the patient. Now focused on making every systematic review searchable, structured, and traceable — so no clinician has to rely on memory when evidence is available.
Specialist in Applied Physiotherapy in Neurorehabilitation with 12 years of experience in private practice. Graduated from secondary pediatric nursing school. Currently completing Master's studies at the Institute in Igalo.
Leading business operations, strategic partnerships, and organizational growth at PhysioSense. Participates in verification of extracted data in the field of neurorehabilitation.
AI extraction with multi-layer verification. Every data point links to the source page in the PDF.
Operated by: PhysioSense
Bar, Montenegro
Extracted data is reviewed by a specialist in applied physiotherapy and pharmaceutical technology before publication. Citations, values, and quotes are verified against original source documents.
PhysioSense is an educational reference tool that presents population-level evidence extracted from published systematic reviews, clinical practice guidelines, and randomized controlled trials. It does NOT diagnose, prognosticate, prescribe, or recommend treatment for individual patients. All evidence is presented at the population level with full source traceability (PMID, page, source-verified quote). The treating clinician always makes the final clinical decision. PhysioSense is classified as an educational resource, not as Medical Device Software (MDSW) under EU MDR or FDA 21 CFR Part 820.
Regulatory basis: FDA 21 CFR 520(o) Clinical Decision Support exemption criteria — the system presents evidence without providing specific clinical action recommendations for individual patients. EU MDCG 2019-11 criteria: the software is not intended to create or modify clinical information and does not provide patient-specific output for individual clinical decision-making.
Cochrane, NICE, ACP, WHO, JOSPT, BJSM — leading evidence from studies and regulatory data, extracted, structured, and cross-referenced in one place.
Start with 10 diagnoses, 8 modules, and full source traceability. Free tier available — no credit card required.
Intervention cards include a "Report Error" button — accuracy is our priority.
PhysioSense · Bar, Montenegro