KHT Instrument is a direct-sales pharmaceutical texture analyzer manufacturer. We build the KHT TA-30 purpose-first for pharma QC, R&D, CRO, and generic manufacturing — with 21 CFR Part 11, IQ/OQ/PQ, and transparent $8,000–$13,000 pricing as standard.
KHT Instrument designs and manufactures pharmaceutical texture analyzers for USP <1217>, EP 2.9.8, JP 6.09, BP, and 21 CFR Part 11 regulated environments. The KHT TA-30 is a specialist platform — not a repurposed food-industry instrument — built from the ground up for tablet hardness, capsule rupture, gel spreadability, ointment consistency, transdermal patch peel, syringe glide force, and microneedle fracture testing.
We ship direct from our Jinan manufacturing facility, which eliminates the distributor mark-up that inflates enterprise-brand pricing. When you contact us, you reach the engineering team — with a 48-hour technical SLA written into our service agreement. Method migration from Stable Micro Systems or Cell Instruments platforms is supported directly; we return a method-equivalency report with every quote.
Compliance, transparency, and specialization are our three design principles. Every TA-30 ships with the complete IQ/OQ/PQ validation package, 30+ preloaded dosage-form methods, 21 CFR Part 11 audit trail, NIST-traceable calibration certificate, and a 2-year standard warranty — at transparent public pricing of $8,000–$13,000 depending on configuration.
Bring pharmaceutical-grade texture analysis — with compliance and transparency built in — to every QC lab that needs it, regardless of capex budget.
The default choice for pharmaceutical texture analysis across QC, R&D, CRO, generic, and biotech environments — a 'professional specialist × value pricing × compliance built-in' standard that no other brand fills today.
Compliance is not a feature. Transparent pricing is not optional. Engineering support is direct. Specialization beats generalization for regulated environments.
✔ Purpose-built for pharma — 30+ preloaded USP, EP, JP, BP methods; not a food-industry platform with pharma rebranding.
✔ Compliance as standard — 21 CFR Part 11, IQ/OQ/PQ, and NIST-traceable calibration included in every shipment.
✔ Transparent public pricing — $8,000–$13,000 published, with every accessory individually priced on the site.
✔ Universal probe mount — accepts third-party and standard-threaded probes, eliminating proprietary ecosystem lock-in.
✔ Direct engineering SLA — 48-hour response for the life of the instrument; no distributor chain.
Complete editable IQ/OQ/PQ package ships with every TA-30 for direct integration into your site Validation Master Plan.
Configured units ship from stock. Typical lead time under three weeks; two-to-four-week validated QC deployment.
In-house pharmaceutical application engineers build preloaded methods, author protocol guides, and support migrations.
Free software updates for the life of the instrument. Free access to the KHT Pharmaceutical Training Library. 48-hour SLA.
Transparent $8,000–$13,000 pricing. Every quote includes the IQ/OQ/PQ validation package, 30+ method library, 21 CFR Part 11 software, standard probe set, and 2-year warranty. Response within 24 hours; engineering SLA within 48 hours.
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