

Empirical testing for global compliance
In-house chromatographic and microbiological assay suites quantify active biomarkers, screen heavy metals, and confirm ingredient identity across every production batch.
Quantified verification thresholds
<0.1 ppm
heavy metal detection floor
100%
incoming lot identity testing
3 Zone
climatic stability testing
24 Hr
COA turnaround on pilot batches


Raw lot to finished release
Analytical verification starts before material enters blending. Raw botanicals, vitamins, and active isolates undergo FTIR spectroscopy and HPLC chromatography to verify purity monographs and eliminate adulteration risks.
Finished dosage units undergo dissolution testing, microbial pathogen plating, and accelerated environmental stress testing to substantiate shelf-life claims in target export jurisdictions.
Review standardized batch dossiers
Obtain unredacted laboratory certificates of analysis, test method summaries, and stability study templates for technical due diligence.
Shinpire Group
Dedicated dual-campus supplement OEM/ODM contract manufacturing.
Operations
Home
Human Nutrition
Pet Health
OEM/ODM Solutions
Facilities
R&D & Quality
Procurement Desk
export@shinpire.com
+86 19141065695
Chengdu High-Tech Industrial Zone, Sichuan, China
Inquiries evaluated within 24 business hours
© 2026 Shinpire Group-Export-grade contract supplement manufacturing compliant with global monographs.
Two Campuses. Zero Cross-Contamination.
