-
E-mail
2577895416@qq.com
-
Phone
19867723812
-
Address
3rd Floor, Building C, Yisai Technology Park, No. 365 Baotian 1st Road, Bao'an District, Shenzhen
Shenzhen Huapu General Technology Co., Ltd
2577895416@qq.com
19867723812
3rd Floor, Building C, Yisai Technology Park, No. 365 Baotian 1st Road, Bao'an District, Shenzhen
Pharmaceutical and biotechnology manufacturers must ensure the quality of materials throughout the entire process from raw materials to finished products. Thermo Scientific TruScan ™ RMThermo Scientific TruScanThrough sealed packaging, reliable material property verification can be provided in real-time as needed within seconds. By using the optional Thermo Scientific TruTools embedded chemometric package, users can establish customized qualitative and quantitative methods suitable for complex material analysis problems.
Description
The TruScan RM analyzer includes an optical system and obtains multivariate residual analysis, providing an effective chemometric solution for material identification using two spectral preprocessing options. The principle of non-destructive aiming sampling of this analyzer is beneficial for the rapid validation of various compounds, including cellulose based products.
Equipping TruTools enhances the functionality of the TruScan RM analyzer as a spectrometer. QA/QC applications include: enhanced identification of similar compound raw materials, multi-component identification, and finished product identification and quantification. The application of Process Analysis Technique (PAT) in distillation includes endpoint determination, reaction monitoring, and powder mixing operations.
TruTools works better when used in conjunction with Solo; The latter is a chemometric software package provided by Eigenvector Research Inc. to allow users to develop models that can be configured onto the TruScan RM analyzer.
TruScan™ RMThermo Scientific TruScanFeatures:
Weight less than 2 pounds (0.9kg)
Durable design; Chemical corrosion resistance and drop resistance
Enhanced compliance with 21CFR Part 11 and cGMP, equipped with biometric login, complex password options, and complete audit trail functionality
Non contact analysis through plastic bags, glass containers, bubble wrap packaging, and transparent adhesive caps
The intuitive workflow can adapt to production environments through PDF batch reports, and data can be easily entered using barcode scanners
Convenient batch management function enables cloning of instruments and identification methods
Suitable for screening counterfeit and inferior drugs
Provide qualification documents (IQ/OQ/PQ) and standard operating procedures
Note: This instrument has not obtained the Medical Device Registration Certificate of the People's Republic of China and cannot be used for clinical diagnosis or treatment related purposes.