Pharmaceuticals

Pharmaceutical chemical procurement requires a higher standard of documentation and quality assurance than general industrial supply. Hasten Chemical meets this standard through:

Supplier qualification: Every pharmaceutical material source undergoes a qualification process including facility audit (or audit documentation review), quality system assessment, and product testing verification. We maintain an approved supplier list and periodic re-qualification schedule.

Lot traceability: Every shipment is traceable from the original manufacturer through our supply chain to your receiving dock. Lot numbers, manufacturing dates, expiration dates, and test results are documented and available for your quality records.

Certificate of Analysis: Every shipment includes a COA from the manufacturer with full analytical results. For products requiring additional testing, we coordinate third-party analytical services to verify specification compliance.

Regulatory documentation: We provide Drug Master File (DMF) references, REACH registration documentation, and other regulatory support materials as required for your product filings.

Our pharmaceutical supply specialists understand that in this industry, the documentation is as important as the product. A chemical that arrives without proper COA documentation is unusable regardless of its quality.