The Indian Pharma supports international sourcing of pharmaceutical formulations from India for importers, distributors, wholesalers, hospitals, NGOs and institutional buyers.
Our sourcing structure covers multiple pharmaceutical dosage forms and therapeutic categories according to product availability and destination-country requirements.
Requirements may include:
We evaluate requirements based on active ingredient, strength, dosage form, quantity, manufacturer preference, destination country and required documentation.
Depending on the manufacturer and product, documentation may include GMP records, WHO-GMP documentation, EU-GMP records, U.S. FDA-related regulatory information, CPP/COPP, Certificate of Analysis and other applicable documents.
Our services can support pharmaceutical importers, distributors, wholesalers, hospitals, NGOs, government procurement teams and other authorized buyers.
Where appropriate manufacturing capabilities are available, contract manufacturing and private-label requirements can also be evaluated separately.
Submit your product specifications and destination country for sourcing evaluation.
Different dosage forms can be evaluated according to product availability.
Yes, bulk requirements can be evaluated.
Yes.
Suitable private-label requirements can be evaluated with appropriate manufacturing partners.
Documentation depends on the product and manufacturer.
