{"id":7436,"date":"2026-09-02T04:15:32","date_gmt":"2026-09-02T04:15:32","guid":{"rendered":"https:\/\/stage-websites.ddismart.com\/vistaar\/?page_id=7436"},"modified":"2026-09-03T11:57:56","modified_gmt":"2026-09-03T11:57:56","slug":"pharma-biotech-regulatory-intelligence-compliance-software","status":"publish","type":"page","link":"https:\/\/stage-websites.ddismart.com\/vistaar\/pharma-biotech-regulatory-intelligence-compliance-software\/","title":{"rendered":"Pharma \/ Biotech"},"content":{"rendered":"<div>\n<p class=\"badge\" style=\"text-align: center;\">Industry Solutions<\/p>\n<h1 style=\"text-align: center;\">Pharma \/ Biotech<\/h1>\n<\/div>\n<div>\n<p style=\"text-align: center; font-size: 1.2rem; color: #b0c0d0; line-height: 1.7; font-weight:400;margin-bottom:20px;\">When it comes to regulatory requirements, you need authoritative and up-to-date information that you can<br \/> rely on. In addition, keeping timely track of ongoing change and introduction of new guidance from different<br \/> countries is important to proactively manage product compliance with different regulatory agencies<\/p>\n<p style=\"text-align: center;color: #00bdb9; font-weight: 500; font-size: 1.15rem;line-height: 1.7;\">At Vistaar, we combine our regulatory intel data sets and workflow technology to ensure you get a full cycle <br \/> regulatory intel and compliance in 1 platform.<\/p>\n<\/div>\n<ul>\n<li>\n<div>\n<h4 style=\"text-align: center;\" class=\"counter\" data-target=\"2000000\" data-suffix=\"+\"><b>0<\/b><\/h4>\n<p style=\"text-align: center;\"class=\"pa2\">Global Regulatory Documents<\/p>\n<\/div>\n<\/li>\n<li>\n<div>\n<h4 style=\"text-align: center;\" class=\"counter\" data-target=\"150\" data-suffix=\"+\"><b>0<\/b><\/h4>\n<p style=\"text-align: center;\"class=\"pa2\">Health Authorities Monitored<\/p>\n<\/div>\n<\/li>\n<li>\n<div>\n<h4 style=\"text-align: center;\" class=\"counter\" data-target=\"100\" data-suffix=\"%\"><b>0<\/b><\/h4>\n<p style=\"text-align: center;\"class=\"pa2\">Cloud-Based Access<\/p>\n<\/div>\n<\/li>\n<li>\n<div>\n<h4 style=\"text-align: center;\" class=\"counter\" data-target=\"24\" data-suffix=\"\/7\"><b>0<\/b><\/h4>\n<p style=\"text-align: center;\"class=\"pa2\">Daily Update Monitoring<\/p>\n<\/div>\n<\/li>\n<\/ul>\n<div>\n<p>    <script>\ndocument.addEventListener(\"DOMContentLoaded\", function () {<\/p>\n<p>  const counters = document.querySelectorAll(\".counter\");\n  const duration = 6000;<\/p>\n<p>  counters.forEach(counter => {<\/p>\n<p>    const target = parseInt(\n      counter.dataset.target,\n      10\n    );<\/p>\n<p>    const suffix =\n      counter.dataset.suffix || \"\";<\/p>\n<p>    const start = performance.now();<\/p>\n<p>    function animate(time) {<\/p>\n<p>      const progress = Math.min(\n        (time - start) \/ duration,\n        1\n      );<\/p>\n<p>      const value = Math.floor(\n        target * progress\n      );<\/p>\n<p>      counter.innerHTML =\n        \"<b>\" +\n        value.toLocaleString() +\n        suffix +\n        \"<\/b>\";<\/p>\n<p>      if (progress < 1) {\n        requestAnimationFrame(animate);\n      }\n\n    }\n\n    requestAnimationFrame(animate);\n\n  });\n\n});\n<\/script>\n<\/div>\n<div>\n<style>\n    .uk-section-primary {\n        background: #dff4fe !important;\n        color: #fff !important;\n    }<\/p>\n<p>    .uk-section-muted {\n       background:#dff4fe !important;\n    }\n    .uk-section-secondary{\n        background:#0d1829 !important;\n    }<\/p>\n<\/style>\n<\/div>\n<div>\n<p class=\"badge\" style=\"text-align: center;\">Platform Features<\/p>\n<h2 style=\"text-align: center; margin-top:0;\">Vistaar Capabilities & Your Benefits<\/h2>\n<p style=\"font-size: 1.15rem; color: #526071; font-weight: 400; text-align: center;\">Comprehensive capabilities engineered for global biopharmaceutical compliance and <br \/> regulatory intelligence.<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/01-regulatory-requirements-pharma.svg\" alt=\"regulatory-requirements-pharma\"><\/p>\n<div>\n<p class=\"para2\">Regulatory requirements for Drugs, Biologics, OTC, and Generics products<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/02-manually-reviewed.svg\" alt=\"manually-reviewed\"><\/p>\n<div>\n<p class=\"para2\">Manually reviewed regulatory summaries covering clinical, technical, QMS\/Quality, market launches, testing standards, submission checklists, fees, labeling, import\/export, marketing, safety\/Vigilance, life cycle requirements, and many more areas in a granular manner<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/03-translated.svg\" alt=\"translated\"><\/p>\n<div>\n<p class=\"para2\">Translated Guidance documents and timely alerts<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/04-global-pharmacovigilance.svg\" alt=\"global-pharmacovigilance\"><\/p>\n<div>\n<p class=\"para2\">Over 2 Million Global regulatory document repository of health authorities\u2019 regulations and guidance, updated daily and provided to you with AI-enabled search for faster and better match<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/06-impact-assessment-pharma.svg\" alt=\"regulatory-requirements-pharma\"><\/p>\n<div>\n<p class=\"para2\">Impact assessment, tracking, compliance matrix, projects\/tasks and reports to o manage full cycle activity from monitoring to alerts review to share\/assign to members, perform global impact assessment and finalize next steps<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/05-document-repository.svg\" alt=\"manually-reviewed\"><\/p>\n<div>\n<p class=\"para2\">Full project management functionality included as standard functionality<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/08-secure-cloud.svg\" alt=\"translated\"><\/p>\n<div>\n<p class=\"para2\">Cloud based with intuitive easy-to-use tool<\/p>\n<\/div>\n<p><img decoding=\"async\" src=\"\/vistaar\/wp-content\/uploads\/2026\/09\/07-integrated-submission.svg\" alt=\"global-pharmacovigilance\"><\/p>\n<div>\n<p class=\"para2\">Using our built-in interfaces, integrate with any of your existing EDMS\/RIM\/Quality systems for exchange data or documents, if needed<\/p>\n<\/div>\n<div>\n<h2 style=\"text-align: center; margin-top:0;\">For more information about Biopharma Regulatory<br \/> Intelligence & Compliance software<\/h2>\n<\/div>\n<p>\n    <a href=\"https:\/\/stage-websites.ddismart.com\/vistaar\/try\/\">Book a Demo<\/a>\n<\/p>\n<div>\n<h2 class=\"hed3\">Related Solutions<\/h2>\n<\/div>\n<ul>\n<li>\n<\/li>\n<li>\n<\/li>\n<\/ul>\n<div>\n<h2 class=\"hed3\">Insights and Updates<\/h2>\n<\/div>\n<div>\n<\/div>\n<div>\n<p class=\"badge\" style=\"text-align: center;\">Got Questions?<\/p>\n<h2 style=\"text-align: center; margin-top:0;\">FAQ's<\/h2>\n<p style=\"font-size: 1.15rem; color: #526071; font-weight: 400; text-align: center;\">Find answers to frequently asked questions about Vistaar's Biopharma platform.<\/p>\n<\/div>\n<ul>\n<li>\n<h3>What is Vistaar's Biopharma Regulatory Intelligence & Compliance software?<\/h3>\n<div>Vistaar is a cloud-based platform that combines global regulatory data with project management workflows. It helps pharmaceutical and biotechnology companies track regulations, review updates, assess global impact, and ensure compliance for drugs, biologics, OTC, and generic products across health authorities worldwide.<\/div>\n<\/li>\n<li>\n<h3>What types of products and regulatory areas does Vistaar cover?<\/h3>\n<div>Vistaar covers drugs, biologics, OTC (over-the-counter), and generic products. It provides manually reviewed summaries across areas such as clinical requirements, technical standards, QMS\/quality, submission checklists, market launches, fees, labeling, import\/export rules, safety\/vigilance, and product lifecycle management.<\/div>\n<\/li>\n<li>\n<h3>How many regulatory documents are available in Vistaar's repository?<\/h3>\n<div>Vistaar features a repository of over 2 million global regulatory documents and health authority guidelines. The database is updated daily and uses AI-enabled search to deliver fast, accurate regulatory matches and translated guidance documents.<\/div>\n<\/li>\n<li>\n<h3>Can Vistaar integrate with existing EDMS, RIM, or Quality systems?<\/h3>\n<div>Yes. Vistaar includes built-in interfaces that allow seamless data and document exchange with existing Regulatory Information Management (RIM), Electronic Document Management Systems (EDMS), and Quality Management Systems (QMS).<\/div>\n<\/li>\n<\/ul>\n<p><!--more--><br \/>\n<!-- {\"name\":\"Home\",\"type\":\"layout\",\"children\":[{\"name\":\"Hero\",\"type\":\"section\",\"props\":{\"animation\":\"slide-left-medium\",\"animation_delay\":false,\"class\":\"banner-background\",\"header_transparent\":false,\"height_offset_top\":false,\"image_position\":\"center-center\",\"image_size\":\"cover\",\"style\":\"secondary\",\"title_breakpoint\":\"xl\",\"title_position\":\"top-left\",\"title_rotation\":\"left\",\"vertical_align\":\"middle\",\"width\":\"default\"},\"children\":[{\"type\":\"row\",\"children\":[{\"type\":\"column\",\"props\":{\"image_position\":\"center-center\",\"position_sticky_breakpoint\":\"m\"},\"children\":[{\"type\":\"text\",\"props\":{\"column_breakpoint\":\"m\",\"content\":\"\n\n<p class=\\\"badge\\\" style=\\\"text-align: center;\\\">Industry Solutions<\\\/p>\\n\n\n<h1 style=\\\"text-align: center;\\\">Pharma \\\/ Biotech<\\\/h1>\",\"css\":\".badge{\\n    display: table;\\n    margin: 0 auto 16px;\\n    background-color: #dff4fe;\\n    color: #0d1829;\\n    font-weight: 700;\\n    font-size: 0.85rem;\\n    text-transform: uppercase;\\n    letter-spacing: 1.5px;\\n    padding: 6px 16px;\\n    border-radius: 20px;\\n    border: 1px solid rgba(0, 189, 185, 0.3);\\n}\\nh1{\\n    font-size: 3.2rem;\\n    font-weight: 900;\\n    line-height: 1.25;\\n    letter-spacing: -0.5px;\\n    color: #ffffff;\\n}\",\"margin\":\"default\",\"text_align\":\"left\"}},{\"type\":\"text\",\"props\":{\"column_breakpoint\":\"m\",\"content\":\"\n\n<p style=\\\"text-align: center; font-size: 1.2rem; color: #b0c0d0; line-height: 1.7; font-weight:400;margin-bottom:20px;\\\">When it comes to regulatory requirements, you need authoritative and up-to-date information that you can<br \/> rely on. In addition, keeping timely track of ongoing change and introduction of new guidance from different<br \/> countries is important to proactively manage product compliance with different regulatory agencies<\\\/p>\\n\n\n<p style=\\\"text-align: center;color: #00bdb9; font-weight: 500; font-size: 1.15rem;line-height: 1.7;\\\">At Vistaar, we combine our regulatory intel data sets and workflow technology to ensure you get a full cycle <br \/> regulatory intel and compliance in 1 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style=\\\"font-size: 1.15rem; color: #526071; font-weight: 400; text-align: center;\\\">Comprehensive capabilities engineered for global biopharmaceutical compliance and <br \/> regulatory intelligence.<\\\/p>\",\"css\":\".badge{\\n    display: table;\\n    margin: 0 auto 16px;\\n    background-color: #dff4fe;\\n    color: #0d1829;\\n    font-weight: 700;\\n    font-size: 0.85rem;\\n    text-transform: uppercase;\\n    letter-spacing: 1.5px;\\n    padding: 6px 16px;\\n    border-radius: 20px;\\n    border: 1px solid rgba(0, 189, 185, 0.3);\\n}\\nh2{\\n    font-size: 2.5rem;\\n    font-weight: 900;\\n    color: #0d1829;\\n    line-height: 1.2;\\n}\",\"margin\":\"\",\"margin_remove_bottom\":false,\"margin_remove_top\":false,\"text_align\":\"center\"}}]}]},{\"type\":\"row\",\"props\":{\"column_gap\":\"medium\",\"css\":\".uk-card-default{\\nbackground-color: #f2f9f5;\\n    padding: 28px 24px;\\n    border-radius: 16px;\\n    border: 1px solid #0d182914;\\n     box-shadow:none 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Drugs, Biologics, OTC, and Generics products<\\\/p>\",\"margin\":\"default\"}}]},{\"type\":\"column\",\"props\":{\"image_position\":\"center-center\",\"position_sticky_breakpoint\":\"m\",\"style\":\"card-default\",\"width_medium\":\"1-4\",\"width_small\":\"1-2\"},\"children\":[{\"type\":\"image\",\"props\":{\"image\":\"wp-content\\\/uploads\\\/2026\\\/09\\\/02-manually-reviewed.svg\",\"image_alt\":\"manually-reviewed\",\"image_svg_color\":\"emphasis\",\"image_width\":52,\"margin\":\"default\"}},{\"type\":\"text\",\"props\":{\"column_breakpoint\":\"m\",\"content\":\"\n\n<p class=\\\"para2\\\">Manually reviewed regulatory summaries covering clinical, technical, QMS\\\/Quality, market launches, testing standards, submission checklists, fees, labeling, import\\\/export, marketing, safety\\\/Vigilance, life cycle requirements, and many more areas in a granular manner<\\\/p>\",\"margin\":\"default\"}}]},{\"type\":\"column\",\"props\":{\"image_position\":\"center-center\",\"position_sticky_breakpoint\":\"m\",\"style\":\"card-default\",\"width_medium\":\"1-4\",\"width_small\":\"1-2\"},\"children\":[{\"type\":\"image\",\"props\":{\"image\":\"wp-content\\\/uploads\\\/2026\\\/09\\\/03-translated.svg\",\"image_alt\":\"translated\",\"image_svg_color\":\"emphasis\",\"image_width\":52,\"margin\":\"default\"}},{\"type\":\"text\",\"props\":{\"column_breakpoint\":\"m\",\"content\":\"\n\n<p class=\\\"para2\\\">Translated Guidance documents and timely alerts<\\\/p>\",\"margin\":\"default\"}}]},{\"type\":\"column\",\"props\":{\"image_position\":\"center-center\",\"position_sticky_breakpoint\":\"m\",\"style\":\"card-default\",\"width_medium\":\"1-4\",\"width_small\":\"1-2\"},\"children\":[{\"type\":\"image\",\"props\":{\"image\":\"wp-content\\\/uploads\\\/2026\\\/09\\\/04-global-pharmacovigilance.svg\",\"image_alt\":\"global-pharmacovigilance\",\"image_svg_color\":\"emphasis\",\"image_width\":52,\"margin\":\"default\"}},{\"type\":\"text\",\"props\":{\"column_breakpoint\":\"m\",\"content\":\"\n\n<p class=\\\"para2\\\">Over 2 Million Global regulatory document repository of health authorities\\u2019 regulations and guidance, updated daily and provided to you with AI-enabled search for faster and better match<\\\/p>\",\"margin\":\"default\"}}]}]},{\"type\":\"row\",\"props\":{\"column_gap\":\"medium\",\"css\":\".uk-card-default{\\nbackground-color: #f2f9f5;\\n    padding: 28px 24px;\\n    border-radius: 16px;\\n    border: 1px solid 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class=\\\"para2\\\">Impact assessment, tracking, compliance matrix, projects\\\/tasks and reports to o manage full cycle activity from monitoring to alerts review to share\\\/assign to members, perform global impact assessment and finalize next steps<\\\/p>\",\"margin\":\"default\"}}]},{\"type\":\"column\",\"props\":{\"image_position\":\"center-center\",\"position_sticky_breakpoint\":\"m\",\"style\":\"card-default\",\"width_medium\":\"1-4\",\"width_small\":\"1-2\"},\"children\":[{\"type\":\"image\",\"props\":{\"image\":\"wp-content\\\/uploads\\\/2026\\\/09\\\/05-document-repository.svg\",\"image_alt\":\"manually-reviewed\",\"image_svg_color\":\"emphasis\",\"image_width\":52,\"margin\":\"default\"}},{\"type\":\"text\",\"props\":{\"column_breakpoint\":\"m\",\"content\":\"\n\n<p class=\\\"para2\\\">Full project management functionality included as standard 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