{"id":761774,"date":"2023-06-06T08:14:50","date_gmt":"2023-06-06T12:14:50","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/agilent-announces-enhanced-xcelligence-rtca-software-pro-to-support-regulatory-compliance-requirements\/"},"modified":"2023-06-06T08:14:50","modified_gmt":"2023-06-06T12:14:50","slug":"agilent-announces-enhanced-xcelligence-rtca-software-pro-to-support-regulatory-compliance-requirements","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/agilent-announces-enhanced-xcelligence-rtca-software-pro-to-support-regulatory-compliance-requirements\/","title":{"rendered":"Agilent Announces Enhanced xCELLigence RTCA Software Pro to Support Regulatory Compliance Requirements"},"content":{"rendered":"

<\/p>\n

Agilent Announces Enhanced xCELLigence RTCA Software Pro to Support Regulatory Compliance Requirements<\/b><\/p>\n

SANTA CLARA, Calif.–(BUSINESS WIRE<\/a>)–Agilent Technologies Inc.<\/a> (NYSE: A) today announced the release of the enhanced xCELLigence RTCA Software Pro Version 2.8<\/a>, an integrated software package for running and analyzing real-time cell analysis data. This improved version enables Agilent xCELLigence Real-Time Cell Analysis (RTCA) systems in GMP-regulated facilities.<\/p>\n

\nThe xCELLigence RTCA Software Pro enables data integrity controls to support regulatory requirements defined in FDA 21 CFR Part 11 and EU GMP Annex 11 for electronic records and electronic signatures, an essential requirement in pharmaceutical and biopharmaceutical manufacturing. New and enhanced features ensure that data and electronic records generated with xCELLigence RTCA systems are trustworthy, authentic, and reliable and meet GMP manufacturing compliance requirements.<\/p>\n

\nThe xCELLigence RTCA system provides an essential functional potency assay in cell therapy development, manufacturing, and safety applications. Agilent instrumentation and software, alongside customer user organization controls, enables customers to meet FDA 21 CFR Part 11<\/a> and other applicable regulatory requirements. This system empowers customers to meet the demands of cell therapy discovery, process development, and QC-release criteria.<\/p>\n

\n\u201cThe addition of compliance features to xCELLigence RTCA Software Pro ensures that Agilent xCELLigence RTCA systems meet the regulatory needs of our valued customers, especially in manufacturing and quality control settings,\u201d said Todd Christian, vice president and general manager of Agilent\u2019s Cell Analysis Division. \u201cThis bridges the regulatory gap, and reinforces Agilent as a leading cell analysis solutions provider to the pharma and biopharma industries.\u201d<\/p>\n

\nAgilent\u2019s key focus is to support customers\u2019 regulatory requirements through our instrumentation and software applications. These solutions for compliant environments support immuno-oncology and cell and gene therapy customers, who are developing key components to address human health concerns, furthering Agilent\u2019s core mission to advance the quality of human life.<\/p>\n

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

\nAgilent Technologies Inc. (NYSE: A) is a global leader in the life sciences, diagnostics, and applied chemical markets, 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 $6.85 billion in fiscal 2022 and employs 18,000 people worldwide. Information about Agilent is available at www.agilent.com<\/a>. To receive the latest Agilent news, please subscribe to the Agilent Newsroom<\/a>. Follow Agilent on LinkedIn<\/a> and Facebook<\/a>.<\/p>\n

\"\"<\/p>\n

View source version on businesswire.com: <\/span>https:\/\/www.businesswire.com\/news\/home\/20230606005547\/en\/<\/a><\/span><\/p>\n

\nNaomi Goumillout
\n
Agilent Technologies
\n
+1.781.266.2819
\n
naomi.goumillout@agilent.com<\/a><\/p>\n

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

INDUSTRY KEYWORDS:<\/b> Software Biotechnology Pharmaceutical Managed Care Health Data Management Health Technology Technology<\/p>\n

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Agilent Announces Enhanced xCELLigence RTCA Software Pro to Support Regulatory Compliance Requirements SANTA CLARA, Calif.–(BUSINESS WIRE)–Agilent Technologies Inc. (NYSE: A) today announced the release of the enhanced xCELLigence RTCA Software Pro Version 2.8, an integrated software package for running and analyzing real-time cell analysis data. This improved version enables Agilent xCELLigence Real-Time Cell Analysis (RTCA) systems in GMP-regulated facilities. The xCELLigence RTCA Software Pro enables data integrity controls to support regulatory requirements defined in FDA 21 CFR Part 11 and EU GMP Annex 11 for electronic records and electronic signatures, an essential requirement in pharmaceutical and biopharmaceutical manufacturing. New and enhanced features ensure that data and electronic records generated with xCELLigence RTCA systems are trustworthy, authentic, and reliable and meet … <\/p>\n

Continue reading “Agilent Announces Enhanced xCELLigence RTCA Software Pro to Support Regulatory Compliance Requirements”<\/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-761774","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nAgilent Announces Enhanced xCELLigence RTCA Software Pro to Support Regulatory Compliance Requirements - 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-enhanced-xcelligence-rtca-software-pro-to-support-regulatory-compliance-requirements\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Agilent Announces Enhanced xCELLigence RTCA Software Pro to Support Regulatory Compliance Requirements - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Agilent Announces Enhanced xCELLigence RTCA Software Pro to Support Regulatory Compliance Requirements SANTA CLARA, Calif.–(BUSINESS WIRE)–Agilent Technologies Inc. (NYSE: A) today announced the release of the enhanced xCELLigence RTCA Software Pro Version 2.8, an integrated software package for running and analyzing real-time cell analysis data. This improved version enables Agilent xCELLigence Real-Time Cell Analysis (RTCA) systems in GMP-regulated facilities. The xCELLigence RTCA Software Pro enables data integrity controls to support regulatory requirements defined in FDA 21 CFR Part 11 and EU GMP Annex 11 for electronic records and electronic signatures, an essential requirement in pharmaceutical and biopharmaceutical manufacturing. 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