Home/Products/Validation & Reclaim Services
Validation & Reclaim Services

Validation & Reclaim Services

Validation & Reclaim Services

Filter retention validation, metal and organic cleanliness analysis, ICP-MS testing and PTFE filter reclaim services.

Validation & Reclaim Services cover filter retention validation, cleanliness analysis, and used-filter reclaim — the three core technical service offerings of JIUNYUAN Technology beyond product sales. Every report is executed under traceable SOPs and qualifies as an official document for internal QA, customer audits, and regulatory validation.

Filter retention validation uses particle challenge testing to measure LRV (Log Reduction Value) and β-ratio, run per ASTM F838, ASTM F795 or customer-specified conditions. Extractables testing uses GC-MS and LC-MS for organic compounds; metallic ion release is measured by ICP-MS across 35+ elements, qualifying filters for semiconductor UPW and pharmaceutical USP <232>/<233> compliance. PTFE reclaim service restores ≥80% of original performance through proprietary cleaning and thermal regeneration, saving 4.2 kg CO₂e per cartridge.

Target clients: semiconductor new-process filter qualification, pharmaceutical pre-cGMP validation, new fab UPW system commissioning, OPEX reduction through reclaim, internal QA audit support, and data evidence for ESG sustainability reporting.

Frequently Asked Questions

What tests are included in filter validation services?
Four main categories: (1) particle challenge testing (β-ratio/LRV per ASTM F838/F795); (2) integrity testing (Bubble Point/Forward Flow); (3) extractables testing (GC-MS/LC-MS for organics, ICP-MS 35 elements for metals); (4) particle shedding (LPC counts). Every report qualifies as regulatory validation or customer audit evidence.
How much performance does PTFE filter reclaim restore?
Proprietary cleaning and thermal regeneration restore ≥80% of original performance, with 2–3 reclaim cycles possible per cartridge. Each cycle saves 4.2 kg CO₂e and reduces procurement cost by 50–60% — suited for non-sterile semiconductor pre-filtration, chemical process, and waste pretreatment applications.
Can the validation reports be used for GMP regulatory certification?
Yes. All tests follow ISO 9001 quality system + traceable SOPs. Reports include raw data, instrument calibration records, and operator sign-off — qualifying as official validation documents for USP <232>/<233>, semiconductor UPW specs, and cGMP pharmaceutical certification.

Need a Custom Solution?

Custom sizes, materials or validation protocols — we can build the solution around your process.

Request Customization