Fast‑track Name Patient access for life‑saving therapies
We specialize in facilitating the import of U.S. FDA-approved or EMA-approved medicines for patients who require them for personal use. Our service ensures that individuals can access internationally approved, high-quality treatments that may not be readily available in their home country, while guiding them through the regulatory, documentation, and logistics process with safety, transparency, and compliance.
What is a Name Patient Program?
A controlled pathway allowing physicians to request access to medicines that aren’t yet locally approved typically for serious or rare conditions, where no satisfactory alternatives exist.
*Timelines vary by country & case complexity.
How it works
We guide patients through every step.
Eligibility & Case Intake
Patient shares authorised prescription and other documents . We confirm local regulations and feasibility.
Manufacturer Liaison
We request supply, pricing, and documentation.
Regulatory Approval
We compile the Named Patient dossier and coordinate permits with the health authority.
Quality & Logistics
Cold‑chain shipping, customs clearance, and etc.
Dispense & Follow‑up
We ensure safe dispensing of approved medicines and provide dedicated follow-up support for every patient.
Renewals
We manage re‑orders, renew permits, and maintain temperature logs for audits.
Typical Documents
| Document | Provided By | Notes |
|---|---|---|
| Physician Request Letter | Clinician | On hospital letterhead |
| Informed Consent | Patient | Signed & dated |
| Product Information (PI) | Manufacturer | Latest version |
| Import Permit | Authority | Country‑specific format |
Expected Timeline
Have a case? We can help today
Dedicated managers respond within hours. Secure, compliant, and transparent from quote to delivery.
