From our laboratory

Formulated in Warsaw.

INFUZE is a clinic with a laboratory attached. Every infusion is compounded in-house under sterile conditions, weighed against a documented protocol, and signed off against your individual case file.

Book consultationSee the protocols
The laboratory

A clinic with a laboratory attached.

Most IV-therapy clinics buy pre-mixed bags from a wholesaler. We compound in-house. The laboratory sits inside the clinic, runs under sterile-compounding standards, and serves only one purpose: the protocol you are about to receive.

Class II laminar flow cabinet
Sterile compounding under HEPA-filtered downflow.
Calibrated analytical balance
Active doses weighed to 0.001 g, calibrated quarterly.
USP-grade water system
Reverse-osmosis water, conductivity verified per batch.
Cold-chain storage
2–8 °C and −20 °C zones with continuous temperature logging.

Bioavailability

Where the dose lands.

Most of an oral supplement never reaches the cell. Intravenous administration bypasses the gut and the first-pass effect of the liver — the dose in the bag is the dose in circulation.

OralIntravenous
Vitamin C
~35%
~98%
Glutathione
~10%
~98%
Magnesium sulfate
~30%
~100%
B-complex
~50%
~100%
NAD⁺
~5%
~100%

Estimates based on published absorption ranges. Individual figures vary with dose, formulation, and patient factors.


Per session

Every dose, weighed and recorded.

Each IV drip produces a written record kept against your individual case file for at least five years. The record covers what was given, when, by whom, and how you responded.

  • Lot number and expiry date for every active ingredient
  • Mass weighed to 0.001 g per active component
  • Final volume, pH, and visual sterility check
  • Operator and witness signatures
  • Vital signs at start and end of infusion
  • Any adverse event, however minor, with follow-up note

INFUZE pharmaceutical-grade ampoules on a clinical paper surface, sealed sterile syringe and folded graphite linen
Sourcing

Pharmaceutical-grade, traceable.

Every active ingredient in an IV drip is pharmaceutical-grade and compliant with the European Pharmacopoeia. We do not use nutraceutical or supplement-grade material at any concentration.

Suppliers are EU-licensed pharmaceutical wholesalers. Each lot arrives with a Certificate of Analysis covering identity, purity, endotoxin level, and sterility. Certificates are retained for five years and made available on request.

Cold-chain ingredients are received and stored under continuous temperature monitoring. Out-of-range excursions trigger quarantine and verification before the lot can be used.


Oversight

Reviewed by physicians.

INFUZE operates as a private medical practice registered with the relevant Polish health authority. Protocols are reviewed and signed off by our medical director — a physician licensed by the Polish Medical Chamber (Naczelna Izba Lekarska).

Each protocol is reviewed quarterly against current literature and clinical experience accumulated across the practice. Material changes to dose, frequency, or indication are documented and applied across all subsequent sessions.

Sterile-compounding practice and clinical procedure are subject to periodic inspection by Sanepid, the Polish public health authority.


Process

From intake to infusion.

01
Consultation
Medical case review covering history, current medications, recent markers, and treatment goals.
02
Protocol selection
Match to one of seven documented protocols, calibrated per case. Dose, cadence and protocol are reviewed against your individual file.
03
Pre-session check
Vital signs and intake confirmation by clinical staff before line placement.
04
In-house mixing
Each IV drip is compounded under sterile conditions immediately before the session. Doses are weighed and recorded against your case file.
05
Infusion under monitoring
Delivered by trained medical staff with continuous observation. Duration matches the protocol — 30 to 180 minutes.
06
Documentation and follow-up
Session record entered against your file. Follow-up review at 7–14 days for ongoing protocols.

Common questions

Common questions.

Is intravenous nutrient therapy supported by evidence?

Specific applications are. High-dose intravenous vitamin C, intravenous magnesium for migraine and pre-eclampsia, intravenous glutathione for hepatic and neurological indications, and NAD⁺ for cellular cofactor restoration are all documented in clinical literature. We do not claim outcomes that are not supported.

Who actually mixes my IV drip?

Trained medical staff under physician supervision, in our laboratory under laminar flow, against the documented protocol for that IV drip. Each batch is signed off by the operator and recorded against your case file.

How is this different from a hospital infusion?

The clinical principles are the same — sterile compounding, dose calibration, monitored delivery. The setting and indication are different: hospital IV is for acute medical need; INFUZE delivers documented protocols around recovery, longevity, and supplementation.

What happens if I have a reaction?

Our staff are trained in infusion-reaction protocols, and emergency medications are kept on-site. Sessions can be paused or stopped at any time. Adverse events are recorded against your file and reviewed.

Do you publish protocols or hold them proprietary?

Standard protocols are documented in writing and shared on request with referring physicians. Case-specific dose adjustments are kept confidential to the individual file.

Where to start

The protocol that fits, calibrated to your case.

Every new client begins with a medical case analysis. The protocol that follows is yours — not selected from a menu.

Book the Consultation