Pharmaceutical
Excipients

Our excipients are supplied against USP-NF, Ph. Eur. and JP monographs where they exist, and every batch ships with a Certificate of Analysis showing compliance with the relevant standard.

Yes. Our technical team advises on particle size, viscosity grade, degree of substitution and functionality so you can match the grade to your tablet, capsule or liquid formulation.

We supply directly compressible grades such as microcrystalline cellulose, lactose monohydrate and modified starches with optimized flowability and compressibility for direct compression routes.

Key products are tested for elemental impurities per ICH Q3D and USP <232>, and we provide nitrosamine risk statements and supporting toxicology data on request.

For principal excipient grades we can support your filing with Drug Master Files, change-control notifications, supplier questionnaires and audit arrangements.

Standard packaging is 25 kg fibre drums with polyethylene liners; big bags and custom palletized export packaging are available for production-scale orders.

R&D quantities start at 1-25 kg depending on the product; commercial orders typically start from 100 kg, and we accommodate trial orders before scale-up.

Yes, evaluation samples are usually dispatched within 3-5 business days together with the latest COA and technical data sheet.

Most excipients are stable for 24-36 months when stored sealed in a cool, dry place; the retest or expiry date is stated on every COA.

Milling, sieving and pre-blending services are available so grades can be tailored to your process requirements and unit operations.