{"id":914562,"date":"2025-12-01T08:18:33","date_gmt":"2025-12-01T13:18:33","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/agilent-announces-21-cfr-part-11-compliance-software-for-xcelligence-rtca-esight\/"},"modified":"2025-12-01T08:18:33","modified_gmt":"2025-12-01T13:18:33","slug":"agilent-announces-21-cfr-part-11-compliance-software-for-xcelligence-rtca-esight","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/agilent-announces-21-cfr-part-11-compliance-software-for-xcelligence-rtca-esight\/","title":{"rendered":"Agilent Announces 21 CFR Part 11 Compliance Software for xCELLigence RTCA eSight"},"content":{"rendered":"

<\/p>\n

Agilent Announces 21 CFR Part 11 Compliance Software for xCELLigence RTCA eSight<\/b><\/p>\n

SANTA CLARA, Calif.–(BUSINESS WIRE<\/a>)–Agilent Technologies Inc<\/a> (NYSE: A) today announced the release of a new 21 CFR Part 11 compliance software<\/a> for the Agilent xCELLigence Real-Time Cell Analysis (RTCA) eSight system<\/a>. The software includes a compliance license and enhanced security features, allowing this multiplex live-cell analysis system to be deployed not only in drug discovery and development labs but now also in GMP-regulated manufacturing and quality control settings. Extending the platform\u2019s use across the pharma and biopharma value chain will help support continuity from early-stage drug discovery and research to production.\n<\/p>\n

\nThe new software is designed to address a rising demand for regulatory-ready digital lab tools in biopharma and cell therapy manufacturing, where data integrity and audit-readiness are critical. Built-in Part 11 compliance and security features have been added to the xCELLigence RTCA eSight, including secure user authentication, electronic signatures, and complete audit trails, assuring users that the data they generate is trustworthy, attributable, and compliant.\n<\/p>\n

\nWith this upgrade, the RTCA eSight offers robust support for regulated environments without compromising on workflow efficiency or data quality. Customers working in GMP environments gain assurance that their electronic records and audit trails meet regulatory standards, helping to streamline audits and support successful regulatory submissions. Extending the same platform used in research to manufacture also helps reduce variability, save time, and simplify compliance across the drug development pipeline.\n<\/p>\n

\n\u201cAdding 21 CFR Part 11 compliance to the Agilent xCELLigence RTCA eSight ensures that customers can rely on their data not just for breakthrough scientific discoveries and insights, but also for regulatory compliance,\u201d said Dr. Knut Wintergerst, vice president and general manager of the Cell and Biomolecular Analysis Division at Agilent. \u201cThis strengthens Agilent\u2019s role as a trusted provider in both discovery and GMP-regulated environments, including manufacturing and quality control.\u201d\n<\/p>\n

\nExpanding the use of RTCA eSight into regulated markets underscores Agilent\u2019s commitment to delivering reliable, compliance-ready, and audit-secure solutions to support customers at every stage in the development of next-generation cell therapies.\n<\/p>\n

About Agilent Technologies<\/b><\/p>\n

\nAgilent Technologies, Inc. (NYSE: A) is a global leader in analytical and clinical laboratory technologies, delivering insights and innovation that help our customers bring great science to life. Agilent\u2019s full range of solutions includes instruments, software, services, and expertise that provide trusted answers to our customers’ most challenging questions. The company generated revenue of $6.95 billion in fiscal year 2025 and employs approximately 18,000 people worldwide. Information about Agilent is available at\u00a0www.agilent.com<\/a>. To receive the latest Agilent news, subscribe to the\u00a0Agilent Newsroom<\/a>. Follow Agilent on\u00a0LinkedIn<\/a>\u00a0and\u00a0Facebook<\/a>.\n<\/p>\n

\"\"<\/p>\n

View source version on businesswire.com: <\/span>https:\/\/www.businesswire.com\/news\/home\/20251201956493\/en\/<\/a><\/span><\/p>\n

Media Contact
\n<\/b>
Kate Coyle
\n
Agilent Technologies
\n
+1 302-633-7490
\n
kate.coyle@agilent.com<\/a><\/p>\n

KEYWORDS:<\/b> California United States North America<\/p>\n

INDUSTRY KEYWORDS:<\/b> Software Research Networks Internet Hardware Pharmaceutical Electronic Design Automation Data Management Consumer Electronics Technology Science Biotechnology Health<\/p>\n

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Agilent Announces 21 CFR Part 11 Compliance Software for xCELLigence RTCA eSight SANTA CLARA, Calif.–(BUSINESS WIRE)–Agilent Technologies Inc (NYSE: A) today announced the release of a new 21 CFR Part 11 compliance software for the Agilent xCELLigence Real-Time Cell Analysis (RTCA) eSight system. The software includes a compliance license and enhanced security features, allowing this multiplex live-cell analysis system to be deployed not only in drug discovery and development labs but now also in GMP-regulated manufacturing and quality control settings. Extending the platform\u2019s use across the pharma and biopharma value chain will help support continuity from early-stage drug discovery and research to production. The new software is designed to address a rising demand for regulatory-ready digital lab tools in biopharma … <\/p>\n

Continue reading “Agilent Announces 21 CFR Part 11 Compliance Software for xCELLigence RTCA eSight”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-914562","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nAgilent Announces 21 CFR Part 11 Compliance Software for xCELLigence RTCA eSight - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/agilent-announces-21-cfr-part-11-compliance-software-for-xcelligence-rtca-esight\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Agilent Announces 21 CFR Part 11 Compliance Software for xCELLigence RTCA eSight - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Agilent Announces 21 CFR Part 11 Compliance Software for xCELLigence RTCA eSight SANTA CLARA, Calif.–(BUSINESS WIRE)–Agilent Technologies Inc (NYSE: A) today announced the release of a new 21 CFR Part 11 compliance software for the Agilent xCELLigence Real-Time Cell Analysis (RTCA) eSight system. The software includes a compliance license and enhanced security features, allowing this multiplex live-cell analysis system to be deployed not only in drug discovery and development labs but now also in GMP-regulated manufacturing and quality control settings. Extending the platform\u2019s use across the pharma and biopharma value chain will help support continuity from early-stage drug discovery and research to production. 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