Clario的封面图片
Clario

Clario

生物技术研究

Philadelphia,Pennsylvania 111,764 位关注者

Transforming Lives by Unlocking Better Evidence | Decentralized clinical trials | Broadest endpoint technology

关于我们

Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019. For more information, visit Clario.com

网站
https://clario.com/
所属行业
生物技术研究
规模
1,001-5,000 人
总部
Philadelphia,Pennsylvania
类型
私人持股
创立
1972
领域
Cardiac Solutions、Medical Imaging、eCOA、Respiratory Solutions、Precision Motion、Specialty Solutions、Clinical Adjudication和Artificial Intelligence

地点

  • 主要

    1818 Market St

    2600

    US,Pennsylvania,Philadelphia,19103

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  • One Cabot Road

    Suite 300

    US,Massachusetts,Medford,02155

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  • 77 Progress Pkwy

    US,Missouri,Maryland Heights,63043

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  • 685 US Highway 202/206

    2nd Floor

    US,New Jersey,Bridgewater,08807

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  • 3750 Monroe Ave

    Suite 600

    US,New York,Pittsford,14534

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  • 1111 Superior Ace

    E, Suite 2400

    US,OH,Cleveland ,44114

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  • 225 West Station Square Drive

    Suite 220

    US,Pennsylvania,Pittsburgh

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  • 1501 Grundy Lane

    Suite A

    US,Pennsylvania,Bristol,19007

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  • 2828 S Corbett Avenue

    Suite 135

    US,Oregon,Portland,97201

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  • Wheatcroft Business Park

    Unit 6

    GB,Nottingham,Nottingham,NG12 4DG

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  • Waversesteenweg 1945 Chaussée de Wavre

    BE,Belgium,Brussels,1160

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  • Sieboldstra?e 3

    DE,Bavaria,Estenfeld,97230

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  • Chemin Louis-Hubert 2

    CH,Geneva,Petit Lancy,1213

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  • Bharathy Street

    452A

    IN,Pondicherry,605001

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  • 2F, 2-13-13 Nihonbashi Kayabacho, Chuo-ku

    JP,Tokyo,103-005

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  • 211 Carnegie Center Drive

    US,New Jersey,Princeton,08540

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  • 777 Mariners Island Blvd

    US,California,San Mateo,94404

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  • Landsberger Stra?e

    290

    DE,Bavaria,Munich,80687

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  • 72 Hammersmith Road

    6th Floor

    GB,London,W14 8UD

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  • No.3, Lane 227, Dong Yu Road, Pudong New Area

    11F

    CN,Shanghai,200126

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  • 3-12-4 Kyobashi, Chuo-ku,

    MAO Building 7F

    JP,Toyko,104-0031

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  • #120P-122P, Belagola Industrial Area

    K.R.S. Road, Metagalli

    IN,Mysore,570016

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Clario员工

动态

  • 查看Clario的组织主页

    111,764 位关注者

    Clario's VP of Medical & Scientific Affairs for Precision Motion, Kristen Sowalsky, PhD, DC, recently participated in a panel discussion at HIMSS Global Health Conference & Exhibition. The session, Revolutionizing Drug Development Through Strategic and Evidence-Driven Digital Health Innovations, focused on how digital health technologies (DHTs) are transforming drug development by improving?motor symptom detection, go/no-go decisions, and real-world evidence collection. Cheers to the panel for an insightful collaboration! Explore Clario's complete solution for measuring digital endpoints of mobility: https://lnkd.in/eFzcnhAY

  • 查看Clario的组织主页

    111,764 位关注者

    ?? Don't miss tomorrow's webinar! ? Join us at 11:00 AM ET for an insightful roundtable on the evolving AI regulatory landscape and its impact on clinical trials. ? What you'll learn:? ?? Key updates from the EU AI Act and FDA's latest AI guidance? ?? Regulatory considerations around fairness, data privacy, safety, and model transparency? ?? Practical strategies for integrating AI technologies into clinical trial workflows ? This is a great opportunity to stay informed and gain valuable insights for your clinical trials. Register now to secure your spot: https://lnkd.in/eshWTz4Y #ClinicalTrials #ResponsibleAI #ClarioAI

  • 查看Clario的组织主页

    111,764 位关注者

    Attending AD/PD 2025? We have lots to share with you!? ? ?? Stop by Clario's booth #50 to find out how we can transform your neuroscience clinical trials with high-quality digital endpoint solutions. And don't miss our poster sessions:? ? Poster 1: Opal sensor equivalency to capture Mobilise-D digital mobility outcomes? Presented by Kristen Sowalsky, PhD, DC, VP, Product Management & Scientific Affairs, Precision Motion? ? Poster 2: Breaking boundaries: How digital movement endpoints outperform clinical scales in tracking disease progression in people with Parkinson’s disease? Presented by Vrutangkumar Shah, Ph.D., Director, Data Science and Biostatistics, Precision Motion? ? Find more event information here: https://lnkd.in/espNUBvz? ? #ADPD2025 #Neuroscience #ClinicalTrials?

    • 该图片无替代文字
  • 查看Clario的组织主页

    111,764 位关注者

    If you missed our LinkedIn Live event discussing the FDA's latest draft guidance on weight-management drugs, the recording is now available!? ? Watch it now to catch up as our experts explore:? ? Key messages from the FDA’s draft guidance for obesity drug development? ? The evolving role of clinical outcome assessments (COAs) and how they can impact labeling claims? ? Practical tips for sponsors on adapting clinical trial design? ? Learn more about the key takeaways and how a comprehensive endpoint strategy can help fulfil regulatory expectations for development of obesity treatments in our article by Todd Rudo, M.D. and Paul Strumph, M.D.: https://lnkd.in/e2b4bwDA

    查看Clario的组织主页

    111,764 位关注者

    ?? The FDA’s new draft guidance for obesity drug development introduces important recommendations that will shape the future of clinical trials in this rapidly expanding market. With the obesity drug market projected to hit $100 billion by 2030, maintaining awareness of the evolving regulatory landscape is crucial for success. ? Join us on March 13 at 10 am ET for an exclusive LinkedIn Live discussion with Todd Rudo, M.D., and Paul Strumph, M.D., as they walk through the key takeaways from the FDA’s new draft guidance. They will discuss its impact on clinical trial design, safety and efficacy endpoints, and regulatory strategy. ? Topics will include: ? Key messages in the FDA guidelines for evaluating weight-management drugs ? The critical role of COAs in supporting labelling claims ? How to navigate regulatory expectations and stay competitive in this fast-growing field RSVP now to join us live and get the insights you need to navigate the changing regulatory landscape. ??

    Navigating the FDA’s New Draft Guidance for Obesity Clinical Trials

    Navigating the FDA’s New Draft Guidance for Obesity Clinical Trials

    www.dhirubhai.net

  • 查看Clario的组织主页

    111,764 位关注者

    ?? The FDA’s new draft guidance for obesity drug development introduces important recommendations that will shape the future of clinical trials in this rapidly expanding market. With the obesity drug market projected to hit $100 billion by 2030, maintaining awareness of the evolving regulatory landscape is crucial for success. ? Join us on March 13 at 10 am ET for an exclusive LinkedIn Live discussion with Todd Rudo, M.D., and Paul Strumph, M.D., as they walk through the key takeaways from the FDA’s new draft guidance. They will discuss its impact on clinical trial design, safety and efficacy endpoints, and regulatory strategy. ? Topics will include: ? Key messages in the FDA guidelines for evaluating weight-management drugs ? The critical role of COAs in supporting labelling claims ? How to navigate regulatory expectations and stay competitive in this fast-growing field RSVP now to join us live and get the insights you need to navigate the changing regulatory landscape. ??

    Navigating the FDA’s New Draft Guidance for Obesity Clinical Trials

    Navigating the FDA’s New Draft Guidance for Obesity Clinical Trials

    www.dhirubhai.net

  • 查看Clario的组织主页

    111,764 位关注者

    ? Our LinkedIn Live event, “Navigating the FDA’s New Draft Guidance for Obesity Clinical Trials,” is one day away. This is your chance to get the inside scoop on the latest regulatory updates shaping the future of obesity drug development. Don't miss this engaging session with our experts Todd Rudo, M.D., Chief Medical Officer, and Paul Strumph, M.D., Diabetes & Metabolism Key Opinion Leader. Save your spot and join us tomorrow at 10:00am ET! ??

    查看Clario的组织主页

    111,764 位关注者

    ?? The FDA’s new draft guidance for obesity drug development introduces important recommendations that will shape the future of clinical trials in this rapidly expanding market. With the obesity drug market projected to hit $100 billion by 2030, maintaining awareness of the evolving regulatory landscape is crucial for success. ? Join us on March 13 at 10 am ET for an exclusive LinkedIn Live discussion with Todd Rudo, M.D., and Paul Strumph, M.D., as they walk through the key takeaways from the FDA’s new draft guidance. They will discuss its impact on clinical trial design, safety and efficacy endpoints, and regulatory strategy. ? Topics will include: ? Key messages in the FDA guidelines for evaluating weight-management drugs ? The critical role of COAs in supporting labelling claims ? How to navigate regulatory expectations and stay competitive in this fast-growing field RSVP now to join us live and get the insights you need to navigate the changing regulatory landscape. ??

    Navigating the FDA’s New Draft Guidance for Obesity Clinical Trials

    Navigating the FDA’s New Draft Guidance for Obesity Clinical Trials

    www.dhirubhai.net

  • 查看Clario的组织主页

    111,764 位关注者

    In a time of increasing complexity in clinical trials, regulatory bodies require more than just robust data—they need consistency, accuracy, and an unbiased evaluation. An independent clinical adjudication process plays a critical role in ensuring endpoint assessments meet these high demands, reducing variability and strengthening the credibility of trial results. ? At Clario, we recognize adjudication not just as helping to comply, but as a strategic advantage. A well-designed adjudication process and robust platform can de-risk regulatory submissions, enhance data integrity, and help accelerate approvals—ultimately bringing life-changing treatments to patients sooner. ? Explore how clinical adjudication can transform trial outcomes: https://lnkd.in/e422vFGA #ClinicalTrials #ClinicalAdjudication

    • 该图片无替代文字
  • 查看Clario的组织主页

    111,764 位关注者

    Join us on March 20 at 11:00 AM ET for an insightful webinar on the AI regulatory landscape and how it's impacting clinical trials. As new and novel uses for artificial intelligence (AI) proliferate, it's crucial to stay ahead of the latest regulations. Our panel of experts will dive into: ? The EUAI Act and FDA’s latest AI guidance ? Key challenges for AI-driven trials such as fairness, privacy, and data accuracy ? Clario's AI Responsible Use principles to mitigate risks ? Practical steps to navigate these regulatory changes Lauren Misztal, General Counsel at Clario, will be joined by Dr. Todd Rudo, Chief Medical Officer, and Marko Topalovic, Chief AI Officer, for this dynamic discussion. ?? Register now to secure your spot: https://lnkd.in/eshWTz4Y

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