How we run a clinic

Mixed for you, on the day of your visit.

Every IV drip is compounded individually in our Warsaw laboratory on the day of your therapy — against the protocol written for your case, never from a pre-mixed bag. Every component is pharmaceutical-grade and EU-sourced, sterile from wholesaler to line, and the same standard applies whether the session is at Klimczaka 8A or at home.

  1. 01
    Licensed staff

    Every line placed by a clinician with a Polish PWZ.

    Infusion sessions at INFUZE are placed and monitored by clinicians with current PWZ (Prawo Wykonywania Zawodu) — the Polish licence to practise. Physician oversight is documented for every protocol. The Consultation is led by our medical director.

  2. 02
    Materials

    Single-use, sterile, CE-marked.

    Butterfly lines, IV sets, syringes, needles and dressings are single-use, sterile, and CE-marked. Nothing in contact with circulation is reused. Sharps are disposed of in compliant containers and collected by a licensed medical-waste handler.

  3. 03
    Compounding

    Mixed on the day of your visit, against your protocol.

    Every IV drip is compounded in our laboratory on the day of your therapy, against the protocol written for your case — never pre-mixed, never kept on a shelf. Doses are weighed on a calibrated analytical balance to 0.001 g under Class II laminar flow, then sealed and brought to the line — in clinic or at home.

  4. 04
    Sourcing

    Pharmaceutical-grade, EU-licensed wholesalers.

    Every active ingredient is pharmaceutical-grade and supplied by EU-licensed pharmaceutical wholesalers — the same sourcing standard whether the session is at Klimczaka 8A or at home. Each lot arrives with a Certificate of Analysis (identity, purity, endotoxin level, sterility), retained on file for five years.

  5. 05
    Component storage

    Each component stored separately, at its own conditions.

    Every active ingredient lives in its own labelled position in the laboratory — at the temperature, light exposure and shelf life specified by the manufacturer. NAD+, glutathione, B-complex and other cold-chain compounds are held in monitored 2–8 °C and −20 °C zones with continuous temperature logging; ambient-stable components sit in controlled room-temperature storage. Out-of-range excursions trigger automatic quarantine before any affected lot is used.

  6. 06
    Emergency response

    Reaction protocols and emergency medications on site.

    Clinical staff are trained in infusion-reaction protocols. Emergency medications including epinephrine, hydrocortisone, antihistamine and oxygen are kept on site. Any session can be paused or stopped at any moment; adverse events are recorded in writing and reviewed by the medical director.

  7. 07
    Insurance

    Professional indemnity in place.

    INFUZE carries professional indemnity insurance covering medical procedures performed both in-clinic and at home addresses across Warsaw. Insurance documentation is available on request to clients and referring physicians.

  8. 08
    Records

    Five-year retention of every case file.

    Every consultation, protocol, dose, and follow-up is recorded against the individual client case file. Records are retained for five years in line with Polish medical-records regulations and EU GDPR. You can request a full copy of your file at any time.

A sealed INFUZE IV drip on a brushed stainless steel tray with a sterile drape and an unlabeled glass vial — individually prepared, ready for the session.

Ready to book?

All documentation — insurance certificate, Certificates of Analysis, the full protocol record — is on file in the clinic and available to review at your session.

Book an IV drip