[{"data":1,"prerenderedAt":80},["ShallowReactive",2],{"industry-life-sciences":3,"industry-use-cases":20},{"id":4,"cta":5,"extension":10,"hero":11,"meta":19,"metaTitle":20,"outcomes":21,"problemImage":41,"problemTitle":20,"problems":42,"seoMeta":46,"slug":49,"socialProofText":50,"solution":51,"solutionImage":62,"stem":63,"useCases":64,"__hash__":79},"industries\u002Findustries\u002Flife-sciences.yml",{"title":6,"description":7,"buttonText":8,"buttonLink":9},"Ready to see your batch operations in one view?","Share a sample of your instrument estate and production workflows and the team will show how FlowFuse would connect, automate, and manage your operations in real time.","BOOK YOUR DEMO","\u002Fbook-demo\u002F","yml",{"eyebrow":12,"eyebrowIcon":13,"heading":14,"description":15,"image":16,"imageAlt":17,"subCta":18},"Life Sciences","academic-cap","Your Electronic Batch Record should be built during production, \u003Cspan class=\"text-red-600\">not assembled after it ends\u003C\u002Fspan>","Connect bioreactors, analytical instruments, LIMS, MES, ELN, and ERP in one place. FlowFuse helps teams automate batch stage coordination, maintain 21 CFR Part 11 data integrity, and carry process logic from development through to commercial GMP production.","\u002Fimages\u002Findustries\u002Flife-sciences.jpg","Wide view of a GMP biopharmaceutical manufacturing facility with stainless steel bioreactors, automated process equipment, and cleanroom production infrastructure.","",{},null,{"title":22,"subtitle":23,"items":24},"Key Outcomes","for Life Sciences Manufacturers",[25,29,33,37],{"svgPath":26,"title":27,"description":28},"document-check","Complete EBR at end of production","with process parameters, quality results, and operator confirmations captured continuously as the batch progresses, QA-ready without post-production compilation.",{"svgPath":30,"title":31,"description":32},"bolt","Accelerate batch stage transitions","by automating hold\u002Frelease decisions and downstream equipment scheduling from LIMS results, eliminating manual coordination delays between operations.",{"svgPath":34,"title":35,"description":36},"arrows-pointing-out","Reduce tech transfer and scale-up rework","with parameterized workflow templates that carry process logic from development through clinical to commercial GMP, configuration, not rebuild.",{"svgPath":38,"title":39,"description":40},"bell-alert","Improve deviation response","with automatic workflow initiation at point of parameter exceedance, full batch context captured without manual reconstruction, CAPA initiated with full linkage.","\u002Fimages\u002Findustries\u002Flife-sciences-problem.svg",[43,44,45],"Scientific instruments operate as isolated systems, process events on one cannot trigger actions on another without manual intervention, consuming scientist and operator time that should be spent on higher-value work.","Electronic Batch Records are assembled after production by pulling data from MES, LIMS, historian, and paper logs, delaying batch release, introducing data integrity risk, and failing the contemporaneous data standard that FDA and EMA inspectors require.","Scale-up and technology transfer require rebuilding operational workflows at each stage, development process logic doesn't carry forward without significant rework, extending time to first GMP batch.",{"title":47,"description":48},"Life Sciences Manufacturing Operations Platform","Connect bioreactors, analytical instruments, LIMS, MES, ELN, and ERP in one place. FlowFuse helps life sciences teams automate batch coordination, maintain data integrity, and accelerate the path from development to GMP production.","life-sciences","Used by biopharmaceutical and life sciences operations teams to automate batch workflows, maintain GMP data integrity, and scale digital initiatives beyond the pilot on top of Node-RED",{"title":52,"benefits":53},"What You Get with FlowFuse",[54,57,59],{"svgPath":55,"text":56},"link","One platform to \u003Cstrong>connect instruments and systems\u003C\u002Fstrong> (bioreactors, analysers, LIMS, MES, ELN) via open protocols, without replacing any of them or renegotiating vendor contracts.",{"svgPath":30,"text":58},"Low-code automation built on Node-RED so scientists and engineers can \u003Cstrong>configure and iterate workflows without vendor dependency or specialist IT\u003C\u002Fstrong>.",{"svgPath":60,"text":61},"rectangle-stack","Dev\u002Ftest\u002Fprod environments that \u003Cstrong>support GMP computer system validation (CSV) requirements\u003C\u002Fstrong> and enable controlled, auditable deployment across scales and sites.","\u002Fimages\u002Findustries\u002Flife-sciences-solution.svg","industries\u002Flife-sciences",{"title":65,"items":66},"Use Cases",[67,71,75],{"image":68,"imageAlt":69,"description":70},"\u002Fimages\u002Findustries\u002Flife-sciences-use-case-1.jpg","Bioreactor, process skid, and analytical instrument connected in a GMP biopharmaceutical manufacturing facility.","\u003Cstrong>Instrument integration and automated batch stage coordination\u003C\u002Fstrong>\u003Cbr>bioreactor phase completion, LIMS in-process results, and equipment scheduling for the next operation connected automatically; hold\u002Frelease decisions executed without manual intervention for standard cases; full stage transition record maintained without separate documentation effort.",{"image":72,"imageAlt":73,"description":74},"\u002Fimages\u002Findustries\u002Flife-sciences-use-case-2.jpg","Electronic Batch Record interface beside a bioreactor in a GMP biopharmaceutical manufacturing facility.","\u003Cstrong>Continuous Electronic Batch Record assembly\u003C\u002Fstrong>\u003Cbr>process parameters, equipment status, operator confirmations, and quality results captured at each step as the batch progresses; EBR complete and QA-ready at end of production with discrepancies flagged in real time, not during post-production review.",{"image":76,"imageAlt":77,"description":78},"\u002Fimages\u002Findustries\u002Flife-sciences-use-case-3.jpg","Deviation management and CAPA workflow displayed on an industrial control panel in a GMP biopharmaceutical manufacturing facility.","\u003Cstrong>Deviation and CAPA workflow\u003C\u002Fstrong>\u003Cbr>parameter exceedance or alarm condition triggers automatic deviation workflow; batch position, process parameters, and equipment state captured at point of event; CAPA initiated directly from deviation record with full data linkage; deviation data aggregated continuously for trend analysis and proactive escalation.","7eLCfEsOp4zh6zJftVmwYPAPheTE9WtidGv9yLq_8Jg",1789472384832]