From Protocol to EDC in Minutes: Streamlining Clinical Trials with BioMeta AI скачать в хорошем качестве

From Protocol to EDC in Minutes: Streamlining Clinical Trials with BioMeta AI

Stop manual EDC builds. Start intelligent automation with BioMeta AI. In this comprehensive walkthrough, we show you how BioMeta AI is revolutionizing clinical trial setup by transforming dense study protocols and complex Excel dictionaries into ready-to-use EDC specifications in minutes. Whether you are a Data Manager, Biostatistician, or Clinical Sponsor, BioMeta AI provides the speed, accuracy, and compliance (21 CFR Part 11) needed to outpace the competition and launch trials faster. In this video, you will learn how to: 1) Automate Ingestion: Convert PDF protocols into structured data instantly. 2) Master the Excel Workflow: Seamlessly import, edit, and version-control data dictionaries. 3) Collaborate in Real-Time: Use our Web-Based Review Portal to annotate and approve specifications with your team. 4) Ensure Compliance: Maintain a complete audit trail and version history for every change. 5) Deploy with One Click: Export to industry-standard formats like CDISC ODM (1.3/2.0), JSON, or push directly via API. Chapter Timestamps 0:00 – Welcome to BioMeta AI: The Future of Clinical Trials 0:20 – Key capabilities of Biometa 0:40 – EDC specification form protocol 1:50 – Reviewing and approving specifications 3:06 – Exporting EDC database 4:32 – Working with Excel and version control 6:17 – Creating custom study template 7:05 – Benefits of Biometa.ai 7:45 – Contact us Why BioMeta AI? Faster Time to Market: Accelerate product timelines by slashing database build times. Accuracy & Consistency: Eliminate human transcription errors with advanced NLP. Compliance Ready: Full traceability and 21 CFR Part 11 support built-in. Connect with Us - Website: biometa.ai LinkedIn:   / talentxpert   #ClinicalTrials #BioMetaAI #EDC #DataManagement #ClinicalResearch #HealthTech #AIinHealthcare #CDISC #21CFRPart11