Ikris Pharma

Legal Documentation

To ensure smooth processing and regulatory compliance for importing medicines under the Named Patient Program, the following documents and details are required:
1. Documents/Details Before Placing an Order Before placing an order, please ensure the following documents and information are available: Identification Proofs: Two valid government-issued ID proofs, including PAN card details, with attested scanned copies. Doctor’s Prescription: A valid prescription from a registered medical practitioner, scanned and clear. Doctor Registration Details: Doctor’s MCI/Medical Council registration number. Doctor Contact: Active mobile number of the prescribing doctor for verification and communication. 2. Documents to be Submitted After Placing an Order Following order placement, the documents below are required to complete the regulatory and compliance formalities: Authority Letter: Authorizing the import of the specific medicine for the named patient. Doctor Consent Letter: Confirming the prescription, indication, and necessity of the medicine for the patient. Drug Utilization Letter: Providing justification for use, treatment plan, and expected duration of therapy. Note: All documents should be scanned clearly, attested where required, and submitted in accordance with regulatory guidelines. Ensuring complete and accurate documentation helps expedite the import process and maintains compliance with Indian regulations.
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