How it works
1. Submit structured details
Include medicine name, strength, dosage form, quantity band, destination country, and organization context. Clear identifiers reduce back-and-forth and support compliant review.
2. Compliance-oriented triage
Inquiries are assessed for licensed buyer fit, regulatory feasibility, and documentation needs. This step is not a clinical review and does not replace institutional approval processes.
3. Quotation or guidance
Where appropriate, next steps may include quotations, referrals to authorized channels, or requests for additional documentation. Timelines vary by product complexity.