Gelatin for capsules,
to the monograph.

Qualification is a documentation exercise.

Capsule and softgel makers do not buy gelatin on price - they buy on the paperwork and the supply chain behind it. Pharmacopoeia conformance (USP / EP), a clean pharmaceutical TSE/BSE declaration, tight physical consistency (Bloom, viscosity, pH), and low bioburden are what let a QA team qualify a source and keep it approved.

Tianran Biotech runs a single-species, single-country supply chain - bovine only, free-range grass-fed Ugandan cattle, veterinary-certified at intake - which removes the porcine cross-contamination and mixed-origin risk that complicate pharma qualification at multi-species plants. Magnus InterGlobe holds stock in the US and is the FDA importer of record. See the full program on Compliance.

USP / EP CoA

Lot Certificate of Analysis to the applicable pharmacopoeia.

TSE / BSE declaration

Pharmaceutical declaration, single-origin grass-fed bovine.

Halal + Kosher

KBHC Cert. 13862; Kosher on request.

150–300 Bloom on contract

Matched to hard-capsule or softgel process.

Capsule gelatin, answered.

Is the gelatin pharmaceutical grade (USP / EP)?

Yes - pharma-grade bovine gelatin to USP and EP monographs is available on contract for hard capsules and softgels, with a lot CoA to the applicable pharmacopoeia and a pharmaceutical TSE/BSE declaration. Food-grade is stocked for nutraceutical and confectionery use.

Do you provide a TSE/BSE declaration?

Yes - a pharmaceutical TSE/BSE declaration accompanies pharma-grade lots, backed by single-species, single-country sourcing from grass-fed Ugandan cattle with veterinary certification at intake.