01
Initial Request
Submit a formal inquiry through our secure platform to begin the medicine access assessment.
05
Sourcing Effort
We coordinate with verified global manufacturers to secure availability for the prescribed specialty therapy.
How Aamrit Facilitates Access
A documentation-led, compliance-first workflow ensuring transparency at every stage of the medicine access journey.
02
Prescription Review
Securely share valid physician prescriptions and patient identity for a legal documentation review.
06
Import Logistics
Managing the complex logistics and documentation for smooth customs and regulatory import clearance.
03
Compliance Review
Our experts evaluate eligibility against international regulatory and medicine access standards.
07
Final Delivery
Ensuring safe delivery to the treating facility with full documentation and audit-ready records.
04
Pathway Approval
Identifying the most appropriate lawful route, such as the direct Named Patient Program pathway.
Note: Documentation requirements vary by case, therapy area, and applicable regulatory pathway. Every request is reviewed as a unique, documentation-led case.
Essential Access Documentation
Aamrit coordinates a document-led workflow to ensure transparency and legal compliance throughout the medicine access process. The following items are foundational for a successful request assessment.
Treating Doctor's Prescription
A valid, formal prescription from a registered medical professional specifying the therapy name, generic title, and dosage requirements.
Doctor Credentials
Professional contact details and hospital affiliation of the prescribing physician to support the regulatory verification process.
Patient Identification Proof
Standard government-issued identity documents to confirm the recipient's credentials and facilitate secure documentation coordination.
Pathway Consent Forms
Signed authorization acknowledging the specific Named Patient access pathway and adherence to compliance protocols.
Clinical Medical Summary
A comprehensive discharge summary or clinical history detailing the diagnosis and treatment rationale for the requested medicine.
Regulatory Documents
Case-specific documentation required by customs and health authorities for the lawful clearance and delivery of critical medicines.
Note: Documentation requirements may vary depending on the therapy area, international supplier response, and current customs regulations. Our team provides detailed guidance for each specific case.