The Indian Pharma supports sourcing of specialty medicines from India for international pharmaceutical importers, distributors, hospitals, specialty healthcare centers, NGOs and authorized institutional buyers.
Specialty medicine requirements often require greater attention to product availability, manufacturer selection, storage conditions, regulatory documentation and destination-market requirements.
Our sourcing capabilities can include products associated with:
Buyers can submit requirements even when a specific product is not listed on our website.
We evaluate the requested medicine, strength, formulation, quantity, manufacturer preference and destination country before identifying appropriate sourcing options.
Depending on the product and manufacturing facility, documentation may include WHO-GMP, EU-GMP, U.S. FDA-related records, CPP/COPP, Certificate of Analysis and other applicable pharmaceutical documentation.
No regulatory credential is assumed to apply to every product.
Hospitals, specialty centers, distributors and institutional procurement teams can submit requirements for specialty medicines.
Where permitted by applicable law, specialty medicines may be sourced through named-patient or special-access mechanisms requiring appropriate medical and regulatory documentation.
Send your medicine requirement and destination country for evaluation.
Specialty medicines generally require specialized clinical, supply or handling considerations and may be used for complex or uncommon conditions.
Yes, institutional requirements can be evaluated.
Rare disease requirements can be submitted for sourcing evaluation.
Yes.
Documentation depends on the product, manufacturer and destination market.
