Clear requirements.
Coordinated supply.
SRA Global Ventures supports pharmaceutical API enquiries through requirement-based product identification, manufacturer coordination, specification alignment and documentation coordination. We connect international buyers with Indian API supply opportunities.
A structured route from enquiry to supply.
Each enquiry is reviewed against the buyer's product, specification, quantity, destination and documentation needs before a product-specific commercial offer is developed.
Understand the requirement
Review API name, exact chemical form, grade or specification, trial and annual quantity, preferred pack, destination and schedule.
Identify supply options
Coordinate with potential Indian manufacturing sources for the requested product and applicable specification.
Align specifications
Review the requested standard and compare it with the manufacturer's specification and available batch CoA.
Coordinate documents
Coordinate available product, batch, manufacturer, stability and regulatory information for buyer evaluation.
Commercial & export support
Develop a product-specific offer and coordinate shipment documentation for the agreed transaction and destination.
Information for a considered product evaluation.
Documentation is coordinated according to the selected manufacturer, API, batch, buyer's request and destination-market requirements.
What can be coordinated?
Documents and technical information may be requested for buyer review, subject to manufacturer availability and authorisation to share.
- Product-specific specification and batch information
- Manufacturer and manufacturing-site details
- Applicable quality and stability support
- Regulatory information, where available
- Export and shipment documents for the transaction
Product quality information
Certificate of Analysis (CoA), product specification, Safety Data Sheet (SDS) and available analytical information.
Source information
Manufacturing licence, applicable GMP evidence, manufacturing-site details and stability support.
Technical declarations
Related substances, residual solvents and applicable elemental impurity, nitrosamine or TSE/BSE information.
Regulatory files
DMF / ASMF or CEP information, where available, with relevant access or authorisation arrangements.
Start with the required standard.
Enquiries may specify a recognised pharmacopoeial standard or an agreed in-house specification. The offered grade must be supported by the selected manufacturer's specification and CoA. Availability of every grade is not implied.
Product-specific packing and shipment planning.
Packaging, storage, transport conditions and shipment paperwork are confirmed against the selected manufacturer's approved system and the requirements of the destination.
Indicative export packaging
Proposed options may include sealed pharmaceutical-grade polyethylene liners within fibre or HDPE drums, with additional moisture or light protection where supported by the approved packaging system.
Documents agreed for each transaction
Shipment documents may include commercial invoice, packing list, certificate or declaration of origin, transport documents and applicable customs, insurance or permit documentation.
Share your API sourcing requirement.
Send the API and exact form, grade or specification, trial and annual quantity, preferred pack, destination and port, required documentation, delivery schedule and trade terms. MOQ, price, lead time, samples and payment terms are confirmed with each quotation.