HIAC 9703+ 實驗室液體顆粒計數器

HIAC 9703+ 液體顆粒計數器能對不同的樣品量進行處理（1 mL 至 1000 mL 都可以，並預先配置 USP、EP、JP 和 KP 試驗常規程序），可以滿足您大多數的應用需求。通過自動沖洗常規程序和測試方法設置向導，操作人員可以在 HIAC 9703+ 液體顆粒計數器上享受更多的無人值守操作。

  • PharmSpec 軟體有效符合  21 CFR Part 11 的監管要求
  • 自動數據庫備份和恢復丟失功能，以此保護有價值的實驗結果數據
  • 提供專家級 SOP 和 IQ/OQ 驗證服務

文件及應用短文

*本產品僅供工業與科學研究使用，不用於臨床診斷  
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HIAC 9703+ 实验室液体颗粒计数器

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Content and Resources

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Changes to USP <1788> Subvisible Particulate Matter
Achieving Compliant Batch Release – Sterile Parenteral Quality Control This paper describes common QC instrumentation compliance elements and gives examples of best practice for instruments used for compliant QC batch release.
Quality Control Electronic Records for 21 CFR part 11 Compliance This paper describes how Quality Control instruments can be optimised for pharmaceutical use, helping to improve the integrity of the data in the final electronic record.
Automating Biopharma Quality Control to Reduce Costs and Improve Data Integrity This paper takes a look at four common quality control procedures and how automation can help improve data integrity by reducing opportunities for human error, whilst also saving time and reducing operating costs.
HIAC 9703+ Sub-Visible Particulate Testing Light Obscuration Testing to USP&lt;787&gt;, &lt;788&gt; and EP 2.9.19

Technical Documents

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