Beijing Bei Fen Tianpu Instrument Technology Co., Ltd
Beijing Beifen Tianpu Instrument Technology Co., Ltd.
Chromatographic Workstation for Pharmaceutical Analysis
Users can be managed at different levels (system administrator, administrator, analyst level 3 and additional level of visitors), and users of different levels have different operating rights after entering the program. The user can close the software interface when temporarily leaving, and need to enter the login password when recovering.
Classification:
Accessories/Consumables
Chromatography workstation
Dedicated Workstation
Hotline:
400-005-7070
Weight
0
Quantity
-
+
Inventory
0
隐藏域元素占位
- Product Description
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- Fully follow the National Pharmacopoeia CommitteeAccording to the requirements of the 2015 edition of Pharmacopoeia and the Drug Evaluation Center of the State Food and Drug Administration, the software has an audit tracking function. Users record important operations on each spectrum and save them together with the spectrum. At the same time, an independent system log is set up to record the time of logging into the software and the name of the operator, the injection time of each sample, the total operation serial number and the name of the generated spectrum file, can fully trace back the detailed process of all experiments,ComplianceGMP specification.
- Users can be managed at different levels (system administrator, administrator, analyst level 3 and additional level of visitors), and users of different levels have different operating rights after entering the program.The user can close the software interface when temporarily leaving, and need to enter the login password when recovering.
- AdoptAll in one's document structure, spectrogram and related contents such as processing methods, quantitative results, remarks, operation records, etc. are all stored in one spectrogram file. At the same time, the file also records the operator's name, injection time, total operation serial number and other information, which fully meets the requirements of FDA on electronic records and electronic signatures in CFR21 Part11, and electronic records and electronic signatures are inseparable,Ensure the integrity, authenticity and accountability of experimental data.
- Software comesThe 3Q authentication module can perform 3Q authentication on the software itself.
- Software can be automatically audited, deleted, replaced or modifiedThe spectrogram file at the Windows time will be automatically listed.
- Sampling data can be outputAIA file or text file for the National Pharmacopoeia Committee of the Chinese medicine fingerprint similarity evaluation system software to read.
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