Do you provide USP-grade certificates for every batch?
Yes. Every USP-grade shipment includes a full Certificate of Analysis (COA) referencing the USP test methods, lot number, manufacturing date, and QA release signature.
Can you supply cGMP-compliant chemicals for drug manufacturing?
Yes. Our manufacturing processes for pharma-grade products are aligned to cGMP principles. We can provide a GMP compliance statement for your supplier qualification files.
What is your change notification policy for pharma products?
We notify customers in advance of any raw material source, supplier, or specification changes that could affect product quality. This is documented in our supplier quality agreement.
Do you offer impurity profiling or residual solvent testing?
Yes, on request. We work with accredited third-party analytical labs to provide extended testing including heavy metals, residual solvents, and related substances.
Can you provide a Drug Master File (DMF) reference?
For certain products, we can provide a DMF reference letter. Contact our technical team for specifics on each product.