贝克曼MET ONE 3400+ 系列空气颗粒计数器

面向 GMP 洁净室的智能环境监测

MET ONE 3400+ 系列为空气洁净室分级和环境监测树立了新的标准。产品以简便性、合规性和高效性为设计理念,可将复杂的标准操作规程(SOP)转化为设备端交互式屏幕工作流程。无需纸质检查表,无需独立软件,即可实现更智能的采样,同时支持 ISO 14644 和 EU GMP Annex 1(欧盟 GMP 附录 1)要求。

主要功能

  • 交互式 SOP 采样地图 可将日常环境监测 SOP 和采样地图直接导入粒子计数器。用户按照屏幕上的分步指引执行操作,从而减少培训时间并降低人为错误。
  • 基于 Web 的远程访问 通过标准网页浏览器即可访问仪器,无需安装额外软件。可执行审核与批准工作流程、管理 SOP 版本,并轻松导出电子记录。
  • 内置审计追踪与合规工具 电子签名和访问控制功能可帮助满足 21 CFR Part 11 合规要求。支持 Microsoft Active Directory,实现集中化用户身份验证与权限管理。
  • 无缝 IT 集成 通过 Microsoft Active Directory 实现简便配置。减少 IT 部署复杂度,帮助用户在现有基础架构内快速部署并安全运行系统。

产品优势

  • 缩短培训时间 交互式地图简化新用户培训和日常操作流程。
  • 降低采样错误 引导式工作流程有助于确保所有采样点的一致性和数据完整性。
  • 简化合规管理 内置安全登录、审计追踪和电子签名功能,为满足 21 CFR Part 11 要求提供支持。
  • 加快审计与报告流程 依托电子记录,可在检查和审计过程中快速定位并筛选所需数据。
  • 无需额外软件 所需功能均集成于仪器之中,可降低整体拥有成本,并加快安装和验证进程。


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选择 MET ONE 3400 Plus 型号

Content and Resources

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Counting Efficiency: MET ONE Air Particle Counters and Compliance to ISO-21501 The one parameter that stands alone as the champion of confusion for defining air particle counter performance is counting efficiency. The purpose of this paper is to present counting efficiency in terms that are easy to understand.
Modern Trends in Non‐Viable Particle Monitoring during Aseptic Processing This paper describes changes and improvements to non‐viable particle monitoring (NVP), sometimes referred to as total particulate monitoring, which is a regulatory requirement during aseptic processing. Aseptic processing is becoming more automated and increasingly important to future products of the biopharmaceutical industry. In the same manner, NVP monitoring is also becoming more automated and increasingly important for contamination risk management during aseptic processing.
Changes to GMP Force Cleanroom Re-Classifications This paper explains the rules of ISO 14644-1:2015, which has substantial revisions impacting both the way the cleanrooms are classified and the performance requirements of the air particle counting instruments used to carry out the classification.
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.
GMP Cleanrooms Classification and Routine Environmental Monitoring The various GMP guidelines and International ISO standards around GMP cleanrooms are complex and often appear to give conflicting advice, leading to confusion and sometimes incorrect interpretation.

技术文件

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