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Agilent Cary WinUV Pharma Revision 5.1.3 – Site Preparation Checklist

Manuals | 2019 | Agilent TechnologiesInstrumentation
Software, UV–VIS spectrophotometry
Industries
Manufacturer
Agilent Technologies

Summary

Importance of Topic


Effective site preparation is essential for the reliable and compliant operation of the Agilent Cary WinUV Pharma system. A well-prepared environment minimizes installation delays, reduces downtime, and ensures that hardware and software perform optimally throughout their service life.

Objectives and Overview


This document provides a comprehensive checklist and specifications to guide customers through the installation of Cary WinUV Pharma Revision 5.1.3. It covers responsibilities, space and utility requirements, computing environment, network scenarios, and software/hardware prerequisites.

Methodology and Instrumentation


The checklist is structured into key areas:
  • Customer Responsibilities and site readiness tasks
  • Software and hardware specification tables
  • Supported installation scenarios (standalone or networked)
  • Required configuration items and administrative steps

Used Instrumentation


  • Agilent Cary 603 UV-Vis Spectrophotometer
  • Agilent Cary 60 UV-Vis Spectrophotometer (firmware 6.4.0.141)

Main Results and Discussion


The site preparation checklist specifies:
  • Supported Cary WinUV Pharma versions and instrument firmware
  • Operating systems: Windows 10 Pro/Enterprise (64-bit), Server 2008 R2 SP1, Server 2012 R2
  • Database and frameworks: Microsoft SQL Server 2014 Express, .NET Framework 3.5 SP1 or 4.5.1
  • Installation scenarios: local standalone vs. networked SCM/SDA configurations
  • Firewall exceptions (.exe processes, TCP/UDP ports), regional settings and backup strategies
  • Minimum hardware: Quad-core CPU, 4 GB RAM (8 GB recommended), 250 GB disk, USB 2.0, 1 Gbps LAN

Benefits and Practical Applications


Adhering to the checklist delivers:
  • Consistent compliance with 21 CFR Part 11 regulations
  • Predictable installation timelines and reduced onsite service costs
  • Stable software and instrument performance over the system’s lifetime
  • Clear responsibilities for IT and laboratory staff during deployment

Future Trends and Opportunities


Emerging developments will further enhance installation and operation:
  • Cloud-based data management integration with LIMS
  • Virtualized deployment and remote installation capabilities
  • Automation of configuration tasks through scripting and orchestration tools
  • Stronger cybersecurity and compliance monitoring features

Conclusion


Thorough site preparation is the cornerstone of a successful Cary WinUV Pharma installation. Following the outlined checklist ensures regulatory compliance, operational reliability, and cost-effective deployment.

References


  • Agilent Spectroscopy Configuration Manager System Requirements
  • Agilent Cary WinUV Pharma Software Installation Instructions for 21 CFR Part 11 Environments
  • Spectroscopy Configuration Manager (SCM) Software, 21 CFR Part 11 Compliance Booklet
  • Agilent Cary WinUV version 5.1.3 Release Notes
  • Agilent Cary UV Pharma Software Status Bulletin
  • Agilent Cary WinUV Software Status Bulletin

Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.

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