Pharma sourcing
Active Pharmaceutical Ingredients & Finished Generic Medicines
Pharmaceutical and OTC sourcing programs managed according to the destination market.
Key takeaways
- 344 listed small-molecule APIs across 14 therapeutic classes, in CP, USP, EP or BP grades, plus 55 biologic actives.
- Finished generic medicines in capsules, tablets, injections, syrups, suspensions, topicals, drops and inhalers.
- COA, MSDS, method of analysis and the manufacturer's GMP certificate are supplied, with DMF or ASMF access where filed.
HOPE Medical sources active pharmaceutical ingredients (APIs) and finished generic medicines for importers, wholesalers and pharmaceutical manufacturers. Products come from audited Chinese manufacturers, and we coordinate samples, documents and shipping. Availability depends on the product, grade and destination registration route, and is confirmed per enquiry.
What we source
- Small-molecule APIs: 344 listed molecules across 14 therapeutic classes, including cardiovascular, anti-infective, antidiabetic, gastrointestinal, central nervous system and analgesic agents, in CP, USP, EP or BP grades.
- Biologic actives: 55 listed peptides, proteins, enzymes, antibodies and nucleic-acid products, as bulk active or finished injectable on request.
- Finished formulations: capsules, tablets, injections, sterile powders for injection, syrups, suspensions, topicals, eye and ear drops, and metered-dose inhalers.
- Intermediates and key starting materials for your own synthesis.
Packaging
Oral solids come in Alu-PVC or Alu-Alu blisters of 10, bottles of 100 to 1000 or bulk drums. Injections come in 1–10 ml ampoules or 10–100 ml vials, liquids in 60, 100 or 120 ml bottles, and topicals in 5–30 g tubes.
Qualification and documents
Each product can be supplied with a certificate of analysis, MSDS, method of analysis and the manufacturer's GMP certificate, with DMF or ASMF access where one is filed. Stability data and samples are available on request. Registration in the destination country remains the importer's responsibility.
What to specify
- Molecule or product name, CAS number and grade
- Quantity and delivery schedule
- Destination market and registration status
- Documents your regulatory team needs
Technical and purchasing information
Pharmaceutical and OTC sourcing programs managed according to the destination market. The final configuration, packaging and supporting documents are confirmed against your order and destination market.
- Product type
- Pharma sourcing
- Application
- Pharmaceutical and OTC sourcing programs managed according to the destination market.
Application and configuration
Confirm the intended use, material, size and model before sample approval or production. Product-specific options are recorded in the quotation and specification sheet.
Packaging and cartons
Packaging, artwork and carton requirements can be reviewed for the selected product. Feasibility is confirmed for the exact order rather than assumed across the category.
Quality and documentation
Available quality and export records vary by product and market. Share the destination and required documents so they can be checked before approval.
Buyer questions, answered
Clear answers for preparing a comparable sourcing request for Pharmaceutical Products.
What are examples of active pharmaceutical ingredients?
An API is the substance in a medicine that produces its effect. Examples from our list include metformin hydrochloride, amlodipine besylate, atorvastatin calcium, amoxicillin trihydrate, paracetamol and omeprazole. Each is supplied with a specification sheet and certificate of analysis.
Must API suppliers be registered with a regulatory authority?
In most regulated markets, the API manufacturer must work under GMP and be named in the medicine's registration file, often through a DMF or ASMF. Requirements differ by country. We share the manufacturer's GMP status and DMF or ASMF access where filed so your regulatory team can assess it.
What documents come with an API or finished-dose shipment?
Typically a certificate of analysis for each batch, MSDS, method of analysis and the manufacturer's GMP certificate, plus the commercial invoice, packing list and certificate of origin. DMF or ASMF access, stability data and registration dossiers are provided where available.
Request the technical datasheet
Include your destination market, target quantity and preferred packaging.
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