{"id":12857,"date":"2025-07-02T09:58:47","date_gmt":"2025-07-02T13:58:47","guid":{"rendered":"https:\/\/clariowebstg.wpengine.com\/?post_type=solutions&p=12857"},"modified":"2025-09-18T14:15:17","modified_gmt":"2025-09-18T18:15:17","slug":"pharma-clinical-trial-solutions","status":"publish","type":"solutions","link":"https:\/\/clario.com\/solutions\/pharma-clinical-trial-solutions\/","title":{"rendered":"Pharma Clinical Trial Solutions"},"content":{"rendered":"
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OVERVIEW<\/p>\n\n\n\n

Driving efficiency, engagement, and scientific excellence<\/h2>\n\n\n\n

Global pharmaceutical companies manage some of the industry\u2019s most complex, high-stakes clinical trials. Clario delivers a single-partner solution that seamlessly integrates scientific expertise, innovative technology and operational excellence – empowering you to accelerate development, minimize risk, and bring transformative therapies to market with confidence.<\/p>\n\n\t<\/div>\n\n<\/div>\n\n <\/div>\n<\/div>\n\n\n

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\"Thought

50+<\/p>

years of experience<\/p><\/div>

\"Consent

30,000+<\/p>

clinical trial opportunities<\/p><\/div>

\"Regulatory

700+<\/p>

FDA and EMA new drug approvals<\/p><\/div>

\"Site

100+<\/p>

countries<\/p><\/div>

\"Drug

70%<\/p>

of FDA and EMA new drug approvals since 2015<\/p><\/div>

\"Patient

24\/7<\/p>

customer and patient support<\/p><\/div><\/div>\n\t<\/div>\n\n<\/div>\n\n <\/div>\n<\/div>\n\n\n

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SOLUTIONS AND EXPERTISE<\/p>\n\n\n\n

At Clario, we simplify the difficult<\/strong><\/h2>\n\n\n\n

We stand as a strategic partner in clinical trials, offering unmatched scientific and regulatory expertise, comprehensive endpoint solutions, and concierge-level support across all phases of drug development.<\/p>\n\n\t<\/div>\n\n<\/div>\n\n <\/div>\n<\/div>\n\n\n

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Scientific and regulatory expertise <\/h3>\n\n\n\n

With decades of experience and a dedicated team of over 140 scientific and medical experts<\/a>, We help optimize endpoint strategy providing industry-leading support in trial design, endpoint selection, and regulatory compliance. <\/strong>Our teams ensure your studies adhere to evolving global regulations, de-risking your development journey and optimizing your path to approval. <\/p>\n\n\n\n

Click on one of the solution areas below to see the related team.<\/p>\n\n\t<\/div>\n\n<\/div>\n\n\n

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Cardiac Solutions<\/h2>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t
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eCOA<\/h2>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t
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Imaging<\/h2>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t
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Precision Motion<\/h2>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t
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Respiratory<\/h2>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n<\/div>\n\t\t<\/div>\n\t<\/div>\n\n<\/div>\n\n <\/div>\n<\/div>\n\n\n
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Comprehensive endpoint solutions <\/h3>\n\n\n\n

We deliver efficacy, safety, and quality of life assessments across all therapeutic areas and trial phases, for seamless continuity throughout your drug development lifecycle from PI through to regulatory submission and beyond.<\/p>\n\n\n\n

Whether you require Imaging<\/a>, eCOA<\/a>, Cardiac<\/a>, or Respiratory<\/a> endpoints, our solutions<\/a> drive reliable, regulatory-grade data to support decision-making and regulatory submissions.<\/strong><\/p>\n\n\n\n

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Scalable, high-volume trial management<\/h3>\n\n\n\n

With an expansive global footprint, we deliver the agility and scale required for today\u2019s most demanding clinical trials.<\/p>\n\n\n\n

Our expert teams seamlessly coordinate multi-continent operations, manage vast patient populations, and optimize high-volume data collection – so your trial progresses on time and on budget. <\/p>\n\n\t\t<\/div>\n\t<\/div>\n\n<\/div>\n\n <\/div>\n<\/div>\n\n\n

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Concierge-level support for global pharma <\/h3>\n\n\n\n

We don\u2019t just provide solutions – we guide you every step of the way.<\/h4>\n\n\n\n

With Clario, you gain a strategic partner that offers hands-on support, from protocol development to regulatory submissions and trial execution. Our expert teams act as an extension of your organization, ensuring you receive white-glove service tailored to your specific study needs. <\/p>\n\n\n\n

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Broad therapeutic area expertise<\/h3>\n\n\n\n

We support clinical trials across a wide range of therapeutic areas<\/a>, so that no matter your indication or trial design, you have access to tailored endpoint solutions. Our deep experience spans neurology, oncology, cardiovascular diseases, metabolic disorders, respiratory, and more – helping pharmaceutical sponsors generate high-quality data to meet regulatory expectations. <\/p>\n\n\t<\/div>\n\n<\/div>\n\n <\/div>\n<\/div>\n\n\n

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Supporting your success at every stage of development<\/h2>\n\n\t<\/div>\n\n<\/div>\n\n\n
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Preclinical and<\/strong> early-phase trials <\/strong><\/h3>\n<\/div><\/div>\n\n\n\n