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"showTitle": true, "titleSize": "lg", "buttonSide": "right", "panelTitle": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022normal\u0022\u003EA connected approach to clinical trial success\u003C/span\u003E", "primaryCta": { "href": "#study-design", "label": "Explore Our Services" }, "panelKicker": "\n", "panelVisual": "paragraphs", "showCaption": false, "showEyebrow": false, "titleWeight": "normal", "secondaryCta": { "href": "/contact", "label": "Talk to Our Team" }, "showSubtitle": false, "cardTextColor": "#ffffff", "panelFontStyle": "default", "panelLogoPlace": "title", "showPanelTitle": false, "panelTitleColor": "#ffffff", "showPanelKicker": true, "panelKickerColor": "", "showSecondaryCta": true }, { "id": "work-together-p9m4mu", "cta": { "href": "/contact", "label": "Learn more" }, "body": "TrialPoint takes a different approach. Applications share a common research environment, so information generated in one part of the study can inform another.", "lede": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003E\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022\u003ETrialPoint\u2122 adapts to the needs of each organization and study, providing the right technology configuration without forcing a one-size-fits-all approach.\u003C/span\u003E\u003C/span\u003E\n\n\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022medium\u0022\u003E\n\u003C/span\u003E\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022medium\u0022\u003E\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EThe platform supports:\u003C/span\u003E\u003C/span\u003E", "logo": "assets/img/logo/tp_logo_dark.svg", "type": "work-together", "color": "#eef6ff", "intro": "TrialPoint\u2122 is more than a collection of clinical research applications. It is a connected ecosystem that brings the people, processes, data, documents, and technology behind a study into one coordinated environment. Each application can stand alone, but greater value comes from how they work together\u2014connecting clinical data with monitoring, safety, imaging, randomization, investigational product management, documents, quality workflows, and reporting.\n\nConfigurable by design, TrialPoint\u2122 allows organizations to start with a single application, integrate with existing systems and partners, or deploy a broader environment across a study, program, or research organization. Applications, workflows, roles, data structures, reports, and dashboards can be configured around the research rather than requiring the research to conform to the technology.\n\nThe result is a connected clinical research ecosystem that keeps information tied to the work that generated it, giving sponsors, CROs, institutions, research networks, and sites greater visibility, traceability, and control from study design through execution and beyond.", "items": [ { "id": "gap-vtfao4", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003EFirst-in-human studies\u003C/span\u003E" }, { "id": "gap-yeuc06", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003EFeasibility and pilot trials\u003C/span\u003E" }, { "id": "gap-7h0qns", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003EPivotal trials\u003C/span\u003E" }, { "id": "copy-qz1lsu", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003ELong-term follow-up\u003C/span\u003E" }, { "id": "copy-vlaeec", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003ELongitudinal studies\u003C/span\u003E" }, { "id": "copy-iar4gk", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003ERegistries\u003C/span\u003E" }, { "id": "p-mnbtog", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003EPost-market surveillance\u003C/span\u003E" }, { "id": "p-hms4qh", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003EInvestigator-initiated research\u003C/span\u003E" }, { "id": "p-fsr7fd", "text": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003EResearch networks and institutional programs\u003C/span\u003E" } ], "pills": [], "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EConfigurable. \u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EModular.\u003C/span\u003E Scalable.\u003C/span\u003E", "closer": "Enter information where it belongs. Use it wherever it is needed.", "color2": "", "follow": "\n", "eyebrow": "The TrialPoint Advantage", "showCta": false, "showLogo": true, "subtitle": "Use what your research requires.", "titleTag": "h2", "showPanel": false, "textColor": "#0a1b46", "titleSize": "lg", "panelColor": "", "panelTitle": "One study. A connected view.", "showCloser": true, "showPoints": true, "logoCaption": "Connected clinical research", "panelColor2": "", "showEyebrow": false, "subtitleTag": "h3", "titleWeight": "normal", "panelTextColor": "", "backgroundStyle": "solid", "panelBackgroundStyle": "none" }, { "id": "connected-applications-jg739n", "cta": { "href": "/contact", "label": "Talk to our team" }, "lede": "TrialPoint\u2122 is designed to support research across the clinical evidence lifecycle, from early development through post-market and real-world evidence generation. The platform can be configured around the requirements of each protocol, program, and organization\u2014providing the structure needed for complex regulated trials while remaining flexible enough to support registries, investigator-initiated research, and multi-study research programs.\n\nStart with the application you need today\u2014or build a connected TrialPoint\u2122 environment that grows with your program.", "type": "connected-applications", "title": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022normal\u0022\u003E\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EThe TrialPoint\u2122 ecosystem.\u003C/span\u003E\u003C/span\u003E", "anchor": "platform", "kicker": "Turn your protocol into an operational framework.", "points": [ { "id": "copy-3kt42d", "icon": "", "title": "\n", "description": "" } ], "eyebrow": "THE TRIALPOINT ECOSYSTEM", "hubLogo": "assets/img/logo/tp_logo_dark.svg", "showCta": false, "hubMicro": "People \u00B7 Processes \u00B7 Data\nTechnology \u00B7 Insights", "hubTitle": "TrialPoint", "products": [ { "id": "cap-ycwcnb", "href": "#platform", "icon": "layers", "slot": "studio", "color": "#7a43f4", "title": "TrialPoint Architect", "color2": "#eee8ff", "bullets": [], "detailBody": "Architect is where your study takes shape in TrialPoint\u2122. Start with a proven protocol template or import your own protocol to establish the foundation for study configuration. Define the study structure, visits, assessments, data requirements, workflows, roles, and other protocol-driven requirements in one place.\n\n\nFrom there, Architect translates the protocol into the applications and workflows needed to execute the study\u2014helping maintain alignment between what the protocol requires and how the study operates. As requirements evolve, configurations can be updated without losing the connection between study design, data collection, and execution.", "description": "Where your study takes shape.", "detailAfter": "", "detailSubtitle": "Protocol, study design and configuration", "showDetailAfter": true, "detailSubheading": "\n", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-i6pjd4", "href": "#platform", "icon": "clipboard-list", "slot": "edc", "color": "#12af76", "title": "EDC", "color2": "#e8f8f2", "bullets": [ { "id": "b-edc-1", "text": "Configurable CRFs and visit schedules" }, { "id": "b-edc-2", "text": "Real-time edit checks and validation" }, { "id": "b-edc-3", "text": "Randomization and stratification" }, { "id": "b-edc-4", "text": "Medical and safety coding" }, { "id": "b-edc-5", "text": "Imaging and document capture" }, { "id": "b-edc-6", "text": "Query management" }, { "id": "b-edc-7", "text": "External and laboratory data" }, { "id": "b-edc-8", "text": "Role-based access and blinding" }, { "id": "b-edc-9", "text": "Visit-window calculations and alerts" }, { "id": "b-edc-10", "text": "Data review and reporting" } ], "detailBody": "TrialPoint\u2122 EDC turns your protocol into a structured environment for clinical data collection and management. Configure CRFs, edit checks, visit schedules, randomization, medical coding, imaging capture, and study-specific data workflows around the requirements of each protocol.\n\n\nBuilt for flexibility, EDC supports simple and complex study designs without forcing every study into the same configuration. Data collection, validation, review, queries, and reconciliation remain connected throughout the study, giving teams a current view of data quality and completeness.\n\n\nAnd because EDC is part of the broader TrialPoint\u2122 environment, clinical data can inform monitoring, safety and clinical event review, investigational product management, study operations, and reporting\u2014connecting the data you collect with the work and decisions it drives.", "description": "Clinical data connected to the rest of your study.", "detailAfter": "\n", "detailSubtitle": "Clinical data connected to the rest of your study.", "showDetailAfter": true, "detailSubheading": "TrialPoint EDC includes:", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-d79ci2", "href": "#platform", "icon": "folder", "slot": "dms", "color": "#f19921", "title": "eTMF \u0026 Essential Documents", "color2": "#fff0da", "bullets": [], "detailBody": "TrialPoint\u2122 eTMF manages essential study documents within the same connected environment as the sites, people, milestones, and activities that generate them. Organize, collect, review, approve, and maintain documents throughout the study while preserving version history, audit trails, and document status.\n\nBecause the eTMF is connected to the broader TrialPoint\u2122 environment, documents can be associated with the relevant study, site, user, activity, or milestone\u2014providing context beyond the document itself. Teams can see what is complete, what is missing, what requires attention, and where documentation gaps may affect study readiness or compliance.\n\nFrom study start-up through closeout, TrialPoint\u2122 eTMF helps maintain a current, inspection-ready record of the study without treating document management as a separate activity that must be reconciled with study operations later.", "description": "Documentation connected to study execution.", "detailAfter": "", "detailSubtitle": "Documentation connected to study execution.", "showDetailAfter": true, "detailSubheading": "\n", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-y8328x", "href": "#platform", "icon": "graduation-cap", "slot": "eqms", "color": "#df37aa", "title": "eQMS \u0026 Learning", "color2": "#fde9f7", "bullets": [], "detailBody": "TrialPoint\u2122 eQMS \u0026 Learning connects controlled documents, training, quality processes, and compliance records with the people and activities they govern. Manage policies, SOPs, work instructions, training requirements, quality events, CAPAs, and related records within a structured, traceable environment.\n\n\nControlled documents can be assigned to the appropriate roles and users, with training requirements triggered as documents are issued or revised. Teams can track acknowledgments, training completion, qualifications, document versions, effective dates, and other compliance requirements\u2014helping ensure people are working from current procedures and have completed the training required for their responsibilities.\n\n\nQuality activities can be managed through configurable workflows for deviations, nonconformances, CAPAs, change control, and other quality processes. Each activity can be connected to the relevant documentation, personnel, training, study, or operational process, creating a clear record from identification through investigation, action, and resolution.\n\n\nBy bringing quality management and learning into the broader TrialPoint\u2122 environment, organizations gain greater visibility into compliance, training status, and quality trends\u2014connecting the procedures that define how work should be performed with the people and activities responsible for carrying it out.", "description": "Connect quality to the work it governs.", "detailAfter": "\n", "detailSubtitle": "Connect quality to the work it governs.", "showDetailAfter": true, "detailSubheading": "\n", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-a0owu4", "href": "#platform", "icon": "brain", "slot": "monitor", "color": "#f08a1c", "title": "Study Management \u0026 Monitoring", "color2": "#fff0df", "bullets": [ { "id": "bullet-copj8m", "icon": "circle-check-big", "text": "Site activation and performance" }, { "id": "bullet-9kjjj7", "icon": "circle-check-big", "text": "Enrollment and retention" }, { "id": "bullet-50ssbh", "icon": "circle-check-big", "text": "Study milestones" }, { "id": "bullet-ckwyk6", "icon": "circle-check-big", "text": "Monitoring activity" }, { "id": "bullet-xwkeaq", "icon": "circle-check-big", "text": "Data completeness" }, { "id": "bullet-z7p7ou", "icon": "circle-check-big", "text": "Safety and clinical event review" }, { "id": "bullet-85gghb", "icon": "circle-check-big", "text": "Investigational product inventory" }, { "id": "bullet-f0q8yr", "icon": "circle-check-big", "text": "Essential documents" }, { "id": "bullet-kq286g", "icon": "circle-check-big", "text": "Open issues and risks" }, { "id": "bullet-zmuc6j", "icon": "circle-check-big", "text": "Vendor and study team activities" }, { "id": "bullet-m2c60x", "icon": "circle-check-big", "text": "Trends, metrics and performance indicators" }, { "id": "bullet-yjwdn3", "icon": "circle-check-big", "text": "Financial reports" } ], "detailBody": "TrialPoint\u2122 Study Management brings the operational work of the study into one connected environment. Manage sites, subjects, milestones, monitoring, issues, tasks, study documentation, and day-to-day activities while maintaining a current view of progress across the program.\n\n\nBecause study management is connected to the broader TrialPoint\u2122 environment, teams can see operational activity in the context of clinical data, enrollment, monitoring, safety, investigational product, documents, and other study information. Rather than assembling status reports from multiple systems, teams can identify delays, emerging risks, outstanding actions, and areas requiring attention as the study progresses.\n\n\nFrom start-up through closeout, TrialPoint\u2122 gives study teams a shared operational picture\u2014helping sponsors, CROs, and research teams coordinate work, maintain accountability, and make informed decisions based on what is happening across the study.", "description": "Connect study operations with clinical insight.", "detailAfter": "\n", "detailSubtitle": "Connect study operations with clinical insight.", "showDetailAfter": true, "detailSubheading": "TrialPoint\u2122 gives project managers and clinical teams real-time visibility into:", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-y5mbtc", "href": "#platform", "icon": "users", "slot": "epro", "color": "#2675ed", "title": "ePRO / eCOA", "color2": "#eaf1ff", "bullets": [], "detailBody": "TrialPoint\u2122 ePRO enables participants to provide patient-reported outcomes, quality-of-life assessments, diaries, questionnaires, symptom information, and other study data remotely through structured, protocol-defined workflows.\n\nConfigure instruments, assessment schedules, reminders, completion windows, and study-specific questionnaires around the requirements of the protocol. Participants can complete required assessments outside the clinic, while study teams can monitor completion, identify missing or overdue assessments, and follow participant-reported information throughout the study.\n\nBecause ePRO is part of the broader TrialPoint\u2122 environment, participant-reported data can remain connected to visits, clinical assessments, safety events, endpoints, and other study data. This gives research teams a more complete view of the participant experience without creating another disconnected source of information to reconcile later.\n\nFrom symptom tracking and daily diaries to validated PRO instruments and quality-of-life assessments, TrialPoint\u2122 ePRO helps capture the participant perspective as an integrated part of the clinical record.\n\n\n", "description": "Keep participants connected. Keep their experience part of the study.", "detailAfter": "", "detailSubtitle": "Keep participants connected. Keep their experience part of the study.", "showDetailAfter": true, "detailSubheading": "\n", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-qy3468", "href": "#platform", "icon": "shield-alert", "slot": "safety", "color": "#e13aa7", "title": "Safety \u0026 Clinical Events", "color2": "#fde8f3", "bullets": [ { "id": "bullet-0ttcei", "icon": "circle-check-big", "text": "Adverse event (AE) and serious adverse event (SAE) capture and management" }, { "id": "bullet-zbm66a", "icon": "circle-check-big", "text": "Adverse device effect (ADE) and serious adverse device effect (SADE) tracking" }, { "id": "bullet-vijkvc", "icon": "circle-check-big", "text": " Event identification and escalation" }, { "id": "bullet-omnlkl", "icon": "circle-check-big", "text": " Structured safety assessments and medical review" }, { "id": "bullet-hu2qge", "icon": "circle-check-big", "text": " Clinical Events Committee (CEC) review and endpoint adjudication" }, { "id": "bullet-70j0is", "icon": "circle-check-big", "text": " Independent, blinded, and multi-reviewer workflows" }, { "id": "bullet-9jv430", "icon": "circle-check-big", "text": " Supporting clinical data, imaging, and document review" }, { "id": "bullet-3j9865", "icon": "circle-check-big", "text": " Coding and event classification" }, { "id": "bullet-loqy1r", "icon": "circle-check-big", "text": " Protocol-defined endpoint review" }, { "id": "bullet-h6odon", "icon": "circle-check-big", "text": " Complete event and decision audit trails" }, { "id": "bullet-k9yc3n", "icon": "circle-check-big", "text": " Safety listings, dashboards, metrics, and reporting" }, { "id": "bullet-cpfikn", "icon": "circle-check-big", "text": " Integration of safety activity with subject, site, and study-level data" } ], "detailBody": "TrialPoint\u2122 brings safety and clinical event management together with the clinical data and supporting documentation needed for informed review. Capture events, supporting records, assessments, follow-up information, and reviewer decisions within a structured, traceable workflow.\n\nBecause safety and event review are connected to the broader TrialPoint\u2122 environment, reviewers can evaluate an event in the context of relevant subject data, visits, procedures, medications, imaging, laboratory results, and other supporting information. This provides a more complete clinical picture without requiring teams to assemble information from multiple systems.\n\nConfigure workflows for safety review, Clinical Events Committee (CEC) review, endpoint adjudication, and other study-specific processes\u2014including reviewer assignments, independent assessments, queries, consensus or adjudication, and final determinations. Every step remains documented and traceable from the initial event through final resolution.", "description": "From event identification through final review.", "detailAfter": "By connecting the event, underlying clinical data, supporting evidence, reviewers, and final determination, TrialPoint\u2122 creates a complete and traceable record of the safety and clinical event review process.", "detailSubtitle": "From event identification through final review.", "showDetailAfter": true, "detailSubheading": "TrialPoint supports:", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-fv86ws", "href": "#platform", "icon": "package", "slot": "device", "color": "#7949ef", "title": "Investigational Product Accountability", "color2": "#eeeaff", "bullets": [ { "id": "bullet-80snzg", "icon": "circle-check-big", "text": " Investigational drugs, devices, and clinical supplies" }, { "id": "bullet-a8kvel", "icon": "circle-check-big", "text": " Product shipment, receipt, and confirmation" }, { "id": "bullet-9ynigo", "icon": "circle-check-big", "text": " Site and depot inventory management" }, { "id": "bullet-7vkxt6", "icon": "circle-check-big", "text": " Lot, batch, serial number, and expiration tracking" }, { "id": "bullet-bxts78", "icon": "circle-check-big", "text": " Kit and device-level accountability" }, { "id": "bullet-osryt5", "icon": "circle-check-big", "text": " Subject assignment and product allocation" }, { "id": "bullet-tbsjvg", "icon": "circle-check-big", "text": " Randomization-linked product assignment" }, { "id": "bullet-6sw93w", "icon": "circle-check-big", "text": " Dispensing and administration tracking" }, { "id": "bullet-qa0qw8", "icon": "circle-check-big", "text": " Product returns, recovery, and disposition" }, { "id": "bullet-xx66vl", "icon": "circle-check-big", "text": " Inventory adjustments and reconciliation" }, { "id": "bullet-lwjhk9", "icon": "circle-check-big", "text": " Resupply thresholds and inventory status monitoring" }, { "id": "bullet-g3o531", "icon": "circle-check-big", "text": " Site-to-site and depot-to-site transfers" }, { "id": "bullet-8gttiw", "icon": "circle-check-big", "text": " Device replacement and exchange tracking" }, { "id": "bullet-vfhpd1", "icon": "circle-check-big", "text": " Role-based access and permissions" }, { "id": "bullet-dry5nu", "icon": "circle-check-big", "text": " Complete product history and audit trail" }, { "id": "bullet-mp1bq4", "icon": "circle-check-big", "text": " Site, subject, and study-level accountability reporting" }, { "id": "bullet-wzf35a", "icon": "circle-check-big", "text": " Final reconciliation and closeout" } ], "detailBody": "Manage investigational drugs, devices, and clinical supplies from shipment and receipt through assignment, dispensing, return, and final reconciliation\u2014maintaining complete accountability throughout the study.", "description": "Know where every product is\u2014and where it\u2019s been.", "detailAfter": "Because IP management is connected to the broader TrialPoint\u2122 environment, product activity can remain linked to the appropriate subject, site, visit, procedure, randomization assignment, and clinical data\u2014creating a traceable record from initial shipment through final disposition.", "detailSubtitle": "Know where every product is\u2014and where it\u2019s been.", "showDetailAfter": true, "detailSubheading": "TrialPoint supports:", "detailSubheadingTag": "strong", "showDetailSubheading": true }, { "id": "cap-axqfnj", "href": "#platform", "icon": "activity", "slot": "site", "color": "#1478f8", "title": "Core Lab Integration", "color2": "#eaf2ff", "bullets": [], "detailBody": "Imaging and associated reports can be captured and managed directly within TrialPoint\u2122 EDC, keeping them connected to the subject, visit, procedure, and clinical data they support. Teams can upload images and reports, track required submissions, manage review status, and maintain a complete audit trail without relying on separate repositories or disconnected workflows.\n\n\nBy keeping imaging within the EDC environment, clinical data, images, interpretations, and related documentation remain part of the same study record. 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Expertise when you need it. Connected when you need both.", "titleTag": "h2", "connector": "Engage Databean for targeted clinical, biostatistical, regulatory, operational, data management, safety, or quality expertise\u2014where and when you need it.\n\nOr, bring Databean expertise and TrialPoint\u2122 technology together in an integrated clinical research model built around your study.\n\n\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003EDatabean brings the expertise. 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The real challenge is identifying\u2014and addressing\u2014the underlying causes.\n\nDatabean evaluates the study across protocol design, sites, enrollment, monitoring, data, vendors, technology, workflows, and governance to identify the root causes affecting performance.\n\nDatabean then builds a prioritized recovery plan, using TrialPoint\u2122 where appropriate to bring study information together, strengthen workflows, and provide the visibility needed to get the study back on track.", "type": "service-offering", "items": [], "theme": "light", "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003ETrial Rescue\u003C/span\u003E", "anchor": "rescue", "kicker": "11", "showIcon": false, "showLink": true, "subtitle": "When a study gets off track, let the evidence show you where to start.", "titleTag": "h2", "connector": "Study recovery isn\u2019t simply about changing vendors or adding resources. It\u2019s about identifying what isn\u2019t working, addressing the root causes, and restoring control of the study.", "linkLabel": "Learn more", "titleSize": "lg", "subtitleTag": "h3", "titleWeight": "normal", "showConnector": true, "connectorTitle": "Regain control of the study.", "showSubheading": true, "showCapabilities": false, "capabilitiesTitle": "Capabilities include:" } ], "description": "Databean clinical research services cover study design, operations, monitoring, data management, safety, quality, real-world evidence, and trial rescue." }, { "id": "page-xu6na2", "slug": "whoweserve", "inNav": true, "title": "Who We Serve | Sponsors, CROs, Sites \u0026 Institutions | Databean", "layout": "landing", "keywords": "clinical trial sponsors, CRO technology platform, research institutions, clinical research sites, site networks, TrialPoint, Databean", "navLabel": "Who we serve", "sections": [ { "id": "photo-path-tjhjs6", "cta": { "href": "/contact", "label": "Let\u2019s talk about your study " }, "lede": "Different research organizations have different priorities. 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"titleTag": "h1", "titleSize": "lg", "showCloser": false, "showEyebrow": false, "subtitleTag": "h3", "titleWeight": "normal", "showSubheading": true }, { "id": "audience-cards-stm29w", "lede": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022 data-scope=\u0022block\u0022\u003EDatabean combines clinical research expertise with TrialPoint\u2122 to meet the specific needs of each organization and study\u2014providing the right mix of expertise and technology while keeping the research connected.\u003C/span\u003E", "type": "audience-cards", "cards": [ { "id": "serve-alkh47", "href": "/whoweserve#sponsors", "icon": "building-2", "title": "Sponsors", "showLink": true, "linkLabel": "Learn more", "description": "Extend your clinical team with experienced specialists and connected technology\u2014without the complexity of managing multiple vendors, systems, and handoffs." }, { "id": "serve-i5zjs5", "href": "/whoweserve#cros", "icon": "users", "title": "CROs", "showLink": true, "linkLabel": "Learn more", "description": "Add configurable clinical technology and specialized expertise that integrate seamlessly with your existing teams, workflows, and delivery model." }, { "id": "serve-dgxekr", "href": "/whoweserve#research", "icon": "graduation-cap", "title": "Research Institutions", "showLink": true, "linkLabel": "Learn more", "description": "Standardize data, workflows, documentation, quality, and oversight across studies and research programs\u2014while maintaining the flexibility each study requires." }, { "id": "serve-ydvs7n", "href": "/whoweserve#sites", "icon": "hospital", "title": "Sites \u0026 Research Networks", "showLink": true, "linkLabel": "Learn more", "description": "Simplify research participation by bringing data collection, documents, training, study workflows, and communication together in one connected environment." } ], "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EDesigned around how you work.\u003C/span\u003E", "eyebrow": "Who we serve", "titleTag": "h2", "titleSize": "md", "showEyebrow": false, "titleWeight": "normal", "showSubheading": true }, { "id": "work-together-quaq1k", "cta": { "href": "/contact", "label": "Let\u0027s talk about your study" }, "body": "\n", "lede": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003EInstead of relying solely on periodic status reports, sponsors can see the study as it develops across:\u003C/span\u003E", "logo": "assets/img/logo/tp_logo_dark.svg", "type": "work-together", "color": "#eef6ff", "intro": "Emerging and established sponsors need access to specialized clinical expertise and technology without having to build every capability in-house.\n\nDatabean can extend your team with targeted expertise in clinical strategy, biostatistics, regulatory affairs, project management, data management, safety, quality, and reporting\u2014or provide an integrated team to support the program from strategy through execution.\n\nTrialPoint\u2122 gives your organization direct visibility into the work behind those services\u2014connecting study activity, data, documents, milestones, issues, and decisions in one environment so you can see how the program is progressing.", "items": [ { "id": "gap-cp65uk", "text": "Enrollment and site performance" }, { "id": "gap-06h4yu", "text": "Clinical data and queries" }, { "id": "gap-q22e5w", "text": "Monitoring and risk management" }, { "id": "gap-7921rh", "text": "Safety and clinical events" }, { "id": "gap-k1ht0i", "text": "Investigational product" }, { "id": "gap-9bda0q", "text": "Essential documents" }, { "id": "p-p4qy1b", "text": "Training and quality" }, { "id": "p-y0d790", "text": "Milestones and study performance" } ], "pills": [ { "id": "pill-2wwl5d", "label": "First-in-human studies" }, { "id": "pill-o61zh4", "label": "Pilot and feasibility studies" }, { "id": "pill-m6g8ie", "label": "Pivotal trials" }, { "id": "pill-91e6tt", "label": "Complex medical device programs" }, { "id": "pill-63tdwl", "label": "Drug and biologic studies " }, { "id": "pill-mctj9h", "label": "Registries" }, { "id": "pill-8di808", "label": "Long-term follow-up " }, { "id": "pill-spojrp", "label": "Post-market research" } ], "title": "Sponsors.", "anchor": "sponsors", "closer": "\n", "color2": "", "follow": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003EYour partners may run the study. You should never lose sight of it.\u003C/span\u003E", "eyebrow": "The TrialPoint Advantage", "showCta": true, "showLogo": false, "subtitle": "Extend your \u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003Eteam without losing visibility.\u003C/span\u003E", "titleTag": "h2", "showPanel": false, "textColor": "", "titleSize": "lg", "panelColor": "", "panelTitle": "Particularly suited for:", "showCloser": true, "showPoints": true, "logoCaption": "Connected clinical research", "panelColor2": "", "showEyebrow": false, "subtitleTag": "h3", "titleWeight": "normal", "panelTextColor": "", "backgroundStyle": "solid", "panelBackgroundStyle": "none" }, { "id": "work-together-z2js67", "cta": { "href": "/contact", "label": "Let\u0027s talk about your operations " }, "body": "TrialPoint takes a different approach. Applications share a common research environment, so information generated in one part of the study can inform another.", "lede": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022\u003EUse TrialPoint\u2122 with your existing teams and processes, or combine the platform with targeted Databean expertise where you need additional support.\u003C/span\u003E\n\n\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022\u003E\n\u003C/span\u003E\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022\u003ETrialPoint can help CROs:\u003C/span\u003E", "logo": "assets/img/logo/tp_logo_dark.svg", "type": "work-together", "color": "#102040", "intro": "CROs don\u2019t necessarily need another CRO.\n\nThey may need better infrastructure.\n\nTrialPoint\u2122 gives CROs a configurable platform for managing clinical data, study operations, monitoring, safety, investigational product, documents, quality, training, and reporting\u2014without relying on a patchwork of separate systems.\n\nWhen additional expertise or capacity is needed, Databean can extend your team with specialized support in biostatistics, data management, safety and CEC, regulatory strategy, and TrialPoint\u2122 configuration.", "items": [ { "id": "gap-be1dg4", "text": "Standardize study delivery" }, { "id": "p-xtb0nk", "text": "Reduce reliance on spreadsheets and disconnected applications" }, { "id": "p-wc8l7t", "text": "Configure workflows around individual protocols" }, { "id": "p-mqm1im", "text": "Give clients greater study visibility" }, { "id": "p-npeyhf", "text": "Support risk-based monitoring" }, { "id": "p-n049sa", "text": "Centralize operational and clinical reporting" }, { "id": "p-7vxa6o", "text": "Scale technology across multiple studies" }, { "id": "p-2paz0o", "text": "Add capabilities without expanding internal infrastructure" } ], "pills": [], "title": "CROs.", "anchor": "cros", "closer": "Enter information where it belongs. Use it wherever it is needed.", "color2": "#ffffff", "follow": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003EYour methodology. Your client relationships. A more connected technology foundation.\u003C/span\u003E", "eyebrow": "The TrialPoint Advantage", "showCta": true, "showLogo": true, "subtitle": "Technology that supports your delivery model\u2014\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003Enot one that replaces it.\u003C/span\u003E", "titleTag": "h2", "showPanel": false, "textColor": "#ffffff", "titleSize": "lg", "panelColor": "", "panelTitle": "One study. A connected view.", "showCloser": true, "showPoints": true, "logoCaption": "Connected clinical research", "panelColor2": "", "showEyebrow": false, "subtitleTag": "h3", "titleWeight": "normal", "panelTextColor": "", "backgroundStyle": "solid", "panelBackgroundStyle": "none" }, { "id": "work-together-69wo4p", "cta": { "href": "/contact", "label": "Let\u0027s explore your program" }, "body": "TrialPoint takes a different approach. Applications share a common research environment, so information generated in one part of the study can inform another.", "lede": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003ETrialPoint supports:\u003C/span\u003E", "logo": "assets/img/logo/tp_logo_dark.svg", "type": "work-together", "color": "", "intro": "Academic research institutions often manage dozens\u2014or hundreds\u2014of studies across different processes, databases, spreadsheets, document repositories, and departmental systems, making consistency, oversight, and visibility difficult to maintain.\n\nThat fragmentation makes oversight difficult and institutional knowledge harder to preserve.\n\nTrialPoint\u2122 provides a configurable research environment that adapts to the needs of individual studies while creating greater consistency, visibility, and oversight across the institution.\n\nStandardize where it adds value while preserving the flexibility each protocol, program, and investigator requires.", "items": [ { "id": "gap-n3mbxd", "text": "Investigator-initiated research" }, { "id": "gap-nigxkm", "text": "Academic sponsored clinical trials" }, { "id": "gap-nolnuk", "text": "Registries" }, { "id": "gap-osouhf", "text": "Observational studies" }, { "id": "gap-5b4e9t", "text": "Long-term follow-up\n" }, { "id": "gap-shzliz", "text": "Research networks" }, { "id": "p-4b89lk", "text": "Departmental research programs" }, { "id": "p-l5ordn", "text": "Sponsored clinical studies" } ], "pills": [], "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EAcademic\u003C/span\u003E Research Institutes.", "anchor": "research", "closer": "Enter information where it belongs. Use it wherever it is needed.", "color2": "", "follow": "TrialPoint\u2122 creates a consistent foundation for data, workflows, documents, training, quality, and reporting while allowing each study to retain the configurations its protocol and research team require.\n\nDatabean can extend internal teams with clinical, biostatistical, data management, and technology expertise\u2014providing targeted support where and when additional capabilities are needed.\n\n\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022semibold\u0022\u003EStandardize the infrastructure\u2014not the science.\u003C/span\u003E", "eyebrow": "The TrialPoint Advantage", "showCta": true, "showLogo": true, "subtitle": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EConnect\u003C/span\u003E research across studies, departments, and programs.", "titleTag": "h2", "showPanel": false, "textColor": "", "titleSize": "lg", "panelColor": "", "panelTitle": "One study. A connected view.", "showCloser": true, "showPoints": true, "logoCaption": "Connected clinical research", "panelColor2": "", "showEyebrow": false, "subtitleTag": "h3", "titleWeight": "normal", "panelTextColor": "", "backgroundStyle": "none", "panelBackgroundStyle": "none" }, { "id": "work-together-z94s4l", "cta": { "href": "/contact", "label": "Let\u0027s explore your research portfolio" }, "body": "TrialPoint takes a different approach. Applications share a common research environment, so information generated in one part of the study can inform another.", "lede": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003EDepending on your program, site personnel can access:\u003C/span\u003E", "logo": "assets/img/logo/tp_logo_dark.svg", "type": "work-together", "color": "#f7f4ff", "intro": "Research sites often work across multiple sponsor systems, portals, document repositories, training environments, and communication channels\u2014creating unnecessary administrative burden for the teams responsible for delivering the research.\n\nEvery additional system adds administrative burden\u2014taking time and attention away from enrolling participants and delivering their care.\n\nTrialPoint\u2122 brings the activities sites perform throughout a study into one connected environment\u2014reducing administrative burden and making it easier for site teams to focus on participants and study execution.", "items": [ { "id": "gap-e0nujz", "text": "eTMF" }, { "id": "copy-hazc8u", "text": "Study and subject workflows" }, { "id": "gap-pp2jbg", "text": "EDC" }, { "id": "gap-gm0r2v", "text": "Visit schedules" }, { "id": "gap-363hsg", "text": "eCOA/ePRO" }, { "id": "gap-b4nn5i", "text": "Investigational product" }, { "id": "gap-s2wz6f", "text": "Essential documents" }, { "id": "p-slozjm", "text": "Training" }, { "id": "p-d9xc8l", "text": "Monitoring activity" }, { "id": "p-r053ns", "text": "Queries and outstanding action items" } ], "pills": [], "title": "Clinical Sites \u0026amp; \u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EResearch Networks\u003C/span\u003E", "anchor": "sites", "closer": "Enter information where it belongs. Use it wherever it is needed.", "color2": "#eef6ff", "follow": "Research networks can use TrialPoint\u2122 to create consistent processes, workflows, and reporting across participating sites while maintaining appropriate access, permissions, and study-level controls.\n\n\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022bold\u0022 data-scope=\u0022block\u0022\u003ELess time navigating systems. More time conducting research.\u003C/span\u003E", "eyebrow": "The TrialPoint Advantage", "showCta": true, "showLogo": true, "subtitle": "Make participating in research easier.", "titleTag": "h2", "showPanel": false, "textColor": "", "titleSize": "lg", "panelColor": "", "panelTitle": "One study. A connected view.", "showCloser": true, "showPoints": true, "logoCaption": "Connected clinical research", "panelColor2": "", "showEyebrow": false, "subtitleTag": "h3", "titleWeight": "normal", "panelTextColor": "", "backgroundStyle": "solid", "panelBackgroundStyle": "none" }, { "id": "bullet-list-e9a996", "type": "bullet-list", "color": "#101f97", "items": [ { "id": "bullet-jn9czs", "icon": "", "text": "Need technology? \u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022normal\u0022\u003EDeploy TrialPoint\u2122 alongside your existing clinical team, CRO, and vendors\u2014without changing the way your study is structured.\u003C/span\u003E" }, { "id": "bullet-vnfg7z", "icon": "", "text": "Need expertise? \u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022normal\u0022\u003EBring in Databean for targeted clinical, biostatistical, regulatory, operational, data management, safety, or quality support\u2014exactly where your team needs it.\u003C/span\u003E" }, { "id": "bullet-d00lnq", "icon": "", "text": "Need both? \u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022normal\u0022\u003ECombine Databean expertise and TrialPoint\u2122 into an integrated clinical research model\u2014configured around your study, your team, and the way you work.\u003C/span\u003E" } ], "title": "One Company. \u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EDifferent Ways to Use It.\u003C/span\u003E", "width": "full", "color2": "#03102d", "framed": false, "layout": "split", "divider": false, "subtitle": "", "titleTag": "h2", "titleSize": "lg", "showPoints": true, "subheading": "Databean and TrialPoint\u2122 adapt to how your organization works\u2014not the other way around.", "titleWeight": "normal", "showSubheading": true, "backgroundStyle": "none" } ], "description": "Sponsors, CROs, research institutions, clinical sites, and networks use Databean and TrialPoint\u2122 for expertise and technology fit to how they run research." }, { "id": "page-3td6in", "slug": "about", "inNav": true, "title": "About Databean | Clinical Research Company Since 2007", "layout": "landing", "keywords": "Databean, about Databean, clinical research company, TrialPoint, clinical trial experts, Jacksonville, founded 2007", "navLabel": "About Databean", "sections": [ { "id": "services-hero-ua2p84", "lede": "Databean was founded in 2007 with a clear purpose: help organizations developing new therapies and technologies conduct better clinical research.\n\nTwo decades of designing and managing complex studies built deep expertise across clinical strategy, biostatistics, regulatory affairs, study operations, monitoring, data management, safety, quality, and reporting.\n\nIt also taught us something important: clinical research technology wasn\u2019t keeping up with the work.\n\nToo many systems were fragmented. Too many workflows were disconnected. And too much time was spent moving information between tools instead of moving research forward.\n\nThat experience shaped what came next: TrialPoint\u2122.", "type": "services-hero", "cards": [], "image": "assets/uploads/1790219611111-ChatGPTImageSep232026at11_13_18PM.png", "steps": [ { "id": "step-0ggtls", "icon": "layers", "lede": "\n", "title": "Architect" }, { "id": "step-nbtuhy", "icon": "clipboard-list", "lede": "\n", "title": "EDC" }, { "id": "step-6jllg6", "icon": "shield-alert", "lede": "\n", "title": "Safety" }, { "id": "step-1vo3sb", "icon": "activity", "lede": "\n", "title": "Monitoring" }, { "id": "step-af084f", "icon": "folder", "lede": "\n", "title": "eTMF/eQMS" } ], "title": "About \u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EDatabean\u003C/span\u003E", "buttons": [], "caption": "\u003Cspan class=\u0022text-weight\u0022 data-weight=\u0022medium\u0022\u003EToday, Databean combines clinical research expertise with TrialPoint to help sponsors, CROs, research institutions, sites, and research networks design, execute, and oversee research through a more connected model.\u003C/span\u003E", "eyebrow": "Clinical research services", "imageAlt": "ChatGPT Image Sep 23, 2026 at 11 13 18 PM", "showLede": true, "subtitle": "\n", "titleTag": "h1", "panelBody": "", "panelLogo": "", "showTitle": true, "titleSize": "md", "buttonSide": "left", "panelTitle": "So we built our own.", "primaryCta": { "href": "#study-design", "label": "Explore Our Services" }, "panelKicker": "THAT TECHNOLOGY BECAME TRIALPOINT\u2122\n", "panelVisual": "steps", "showButtons": false, "showCaption": true, "showEyebrow": false, "titleWeight": "normal", "secondaryCta": { "href": "/contact", "label": "Talk to Our Team" }, "showSubtitle": false, "cardTextColor": "", "panelFontStyle": "semibold", "panelLogoPlace": "title", "showPanelTitle": true, "panelTitleColor": "", "showPanelKicker": true, "panelKickerColor": "#ffffff", "showSecondaryCta": false }, { "id": "work-together-b51y14", "cta": { "href": "/contact", "label": "Learn more" }, "body": "TrialPoint takes a different approach. Applications share a common research environment, so information generated in one part of the study can inform another.", "lede": "Our teams needed better ways to manage clinical data, sites, monitoring, safety, investigational product, documents, quality, and study oversight.", "logo": "assets/img/logo/tp_logo_dark.svg", "type": "work-together", "color": "", "intro": "", "items": [ { "id": "gap-35pbqu", "text": "Teams create spreadsheets to fill the gaps." } ], "pills": [], "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EBuilt f\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003Erom the ground up.\u003C/span\u003E\u003C/span\u003E", "closer": "Enter information where it belongs. Use it wherever it is needed.", "color2": "", "follow": "Rather than continuing to connect separate applications and spreadsheets around every new study, we began building technology around the way clinical research actually operates.\n\nThat experience continues to shape TrialPoint today.\n\nClinical experts help define what the technology needs to accomplish. Technology gives our clinical teams better ways to execute, oversee, and understand the study.\n\nThe platform gets better because we understand the research.\u2028The research gets better because we understand the technology.", "eyebrow": "The TrialPoint Advantage", "showCta": false, "showLogo": true, "subtitle": "TrialPoint\u2122 wasn\u2019t designed in isolation. It grew out of the realities of clinical research.", "titleTag": "h2", "showPanel": false, "textColor": "", "titleSize": "lg", "panelColor": "", "panelTitle": "One study. A connected view.", "showCloser": false, "showPoints": false, "logoCaption": "Connected clinical research", "panelColor2": "", "showEyebrow": false, "subtitleTag": "h3", "titleWeight": "normal", "panelTextColor": "", "backgroundStyle": "none", "panelBackgroundStyle": "none" }, { "id": "value-g6hluk", "cta": { "href": "/contact", "label": "Talk to our team" }, "lede": "\n", "type": "value", "items": [ { "id": "item-u0t2uk", "href": "/contact", "icon": "brain", "color": "#1268ff", "title": "Clinical Research Expertise", "color2": "#8657ff", "iconFill": "gradient", "showLink": true, "subtitle": "", "linkLabel": "Learn more", "description": "Databean brings experienced professionals across the disciplines required to move clinical research forward\u2014from study design and regulatory strategy through execution, data management, monitoring, safety, quality, analysis, and reporting.\n\nEngage us for a specific capability or as an integrated extension of your team." }, { "id": "item-7t9okw", "href": "/contact", "icon": "layers", "color": "#1268ff", "title": "TrialPoint\u2122 Technology", "color2": "#8657ff", "iconFill": "gradient", "showLink": true, "subtitle": "", "linkLabel": "Learn more", "description": "TrialPoint connects the applications, workflows, data, documents, and insights required to conduct and oversee clinical research.\n\nDeploy the technology independently with your existing team and partners or combine it with Databean services.\n\nTogether, they create a more connected approach to clinical research." } ], "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EOne Company. Two Complementary Strengths\u003C/span\u003E", "eyebrow": "Value delivered", "showCta": false, "subtitle": "\n", "titleTag": "h2", "showEyebrow": false, "subtitleTag": "h3" }, { "id": "bullet-list-6gi5oi", "type": "bullet-list", "color": "#dfecfb", "items": [ { "id": "bullet-jn9czs", "icon": "", "text": "Databean has always been drawn to research that requires thoughtful study design, specialized expertise, and flexibility.\n" }, { "id": "bullet-vnfg7z", "icon": "", "text": "Our experience spans medical devices, drugs and biologics, novel technologies, complex therapeutic areas, and studies ranging from first-in-human through pivotal and post-market research." }, { "id": "bullet-d00lnq", "icon": "", "text": "We understand that different programs require different operating models." }, { "id": "bullet-mallz4", "icon": "", "text": "That\u2019s why both our services and our technology are designed to adapt around the research\u2014not force the research into a predetermined model." } ], "title": "Designed for \u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EComplex Research\u003C/span\u003E", "width": "full", "color2": "#eef6ff", "framed": false, "layout": "split", "divider": false, "subtitle": "Clinical programs slow down when teams, systems, and information are disconnected.", "titleTag": "h2", "titleSize": "lg", "showPoints": true, "subheading": "Because the most interesting studies rarely fit neatly into a template.", "titleWeight": "normal", "showSubheading": true, "backgroundStyle": "solid" }, { "id": "capabilities-91vdwa", "lede": "Databean doesn\u2019t require a single delivery model.\n\nWe can lead an integrated clinical program, provide specialized expertise alongside an existing CRO or internal team, or deploy TrialPoint as the technology foundation supporting your own processes.\n\nThat flexibility allows organizations to build the model appropriate for the study rather than buying more services or technology than they need.", "type": "capabilities", "items": [ { "id": "item-kdxajz", "href": "/contact", "icon": "workflow", "title": "Workflow automation", "showLink": false, "subtitle": "", "linkLabel": "Learn more", "description": "Add a short description." } ], "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003EBuilt to Work \u003C/span\u003EWith Your Team", "eyebrow": "Platform capabilities", "showItems": false, "showEyebrow": false, "titleWeight": "normal" } ], "description": "Since 2007, Databean has combined experienced clinical researchers with TrialPoint\u2122 so life-science teams can design, execute, and oversee complex studies." }, { "id": "page-contact", "slug": "contact", "inNav": true, "title": "Contact Databean | Talk With Clinical Research Experts", "layout": "contact", "keywords": "contact Databean, clinical research consultation, TrialPoint demo, clinical research experts, clinical trial technology", "navLabel": "Talk to our team", "sections": [ { "id": "contact", "lede": "Tell us how your organization operates today and where teams, workflows, or systems are creating friction. We\u2019ll bring the right clinical and technology leaders into the conversation.", "type": "contact", "email": "info@databean.com", "phone": "\u002B1 844 664 3001", "title": "\u003Cspan class=\u0022text-fill\u0022 data-fill=\u0022gradient\u0022\u003ETalk with our clinical research and technology experts.\u003C/span\u003E", "points": [ { "id": "cp-1", "label": "CRO and research-institution platform enablement" }, { "id": "cp-2", "label": "Biotech and medical-device study support" } ], "address": "5011 Gate Pkwy, Bldg. 100, Ste. 100\nJacksonville, FL 32256", "eyebrow": "Let\u2019s build what\u2019s next", "titleSize": "lg", "showEyebrow": true, "titleWeight": "normal" } ], "description": "Talk with Databean about TrialPoint\u2122 or clinical research services. Tell us where teams, workflows, or systems are creating friction in your study." } ], "version": 2, "updatedAt": "2026-10-01T20:33:49.9304740\u002B00:00" }