Pharmaceutical APIs & Bulk Drugs Supplier

Sourcing 123+ active pharmaceutical ingredients with regulatory documentation support for India, US, and EU markets.

Note: The above products are not for sale where patents are applicable and still valid.

Frequently Asked Questions

What is an API or bulk drug?
An active pharmaceutical ingredient (API) is the therapeutic compound in a medicine responsible for its pharmacological effect. We source and procure APIs in bulk quantities for pharmaceutical manufacturing, formulation, and clinical development.
Do you supply small quantities for R&D or clinical trials?
Yes. We source both research quantities (gram to kilogram scale) for preclinical and clinical development, and commercial bulk volumes (kilograms to metric tonnes) for manufacturing. Contact us with your scale; we will identify the appropriate manufacturer and provide tiered pricing.
What regulatory documentation supports your APIs?
All APIs include Certificate of Analysis (CoA), MSDS, technical specification sheets, and batch traceability. US Drug Master File (USDMF), European Drug Master File (EDMF), CEP (Certified Exported Product), WHO-GMP certificates, and regulatory dossiers are available for supported products.
Can you help with regulatory dossier preparation for new market entry?
Yes. Our team assists with regulatory requirements documentation, including USDMF filing support, DMF type selection, regulatory compliance verification, and market-specific documentation for US, EU, India, Brazil, and other regulated markets.
What are typical API sourcing timelines?
Standard sourcing: 4-8 weeks from order confirmation. Expedited sourcing (for established products): 2-4 weeks. Emergency sourcing (for manufacturing disruptions): contact us immediately; we will assess availability and feasibility.

About This Category

Sumsahi Kemicals, Delhi-based pharmaceutical sourcing house (founded 2003), supplies 123+ APIs and bulk drugs from WHO-GMP and Schedule M certified manufacturers in China, Germany, Korea, Japan, Taiwan, India. APIs include new chemical entities, generic APIs, advanced intermediates. All products include Certificate of Analysis (CoA), CoPP, MSDS, technical specs. USDMF, EDMF, CEP, WHO-GMP documentation available. Sourcing timeline: 4-8 weeks standard; 2-4 weeks expedited. Contact: +91 98104 45252 or [email protected].