We're excited to send members of our team in India to SCDM! At this event, attendees explore the multifaceted nature of Risk-Based Data Management, addressing the challenges of data security, privacy, and regulatory compliance. #SCDM #datamanagement #regulatorycompliance Thiyagarajan Ramasamy, Rajesh Muvva Biswadhip Pai, MSc, MRes, IPBA (IIM Indore)
关于我们
End-to-End Service Provider for Medical Device Companies When it comes to accelerating your healthcare product ideas into reality, Veranex stands out as the accomplished expert. We offer a revolutionary approach with our integrated service offering for medical technologies by providing comprehensive expertise to healthcare product companies. Our agile solutions ensure that you can develop life changing medical technologies that impact healthcare practitioners and patients worldwide. What We Offer: ? Product Design & Engineering ? Preclinical ? CRO & Consulting Services For more information, visit https://veranex.com/
- 网站
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https://www.veranex.com
Veranex的外部链接
- 所属行业
- 医疗设备制造业
- 规模
- 1,001-5,000 人
- 总部
- Raleigh,North Carolina
- 类型
- 私人持股
- 创立
- 2021
- 领域
- Software validation、Industry design、Engineering、Human factors、Testing laboratory、Medical writing、IVDR/MDR、Patient recruitment、Post market、Data management、Biostatistics、Health economics、Outcomes research、Reimbursement、Machine learning、Artificial intelligence、Technology service platform、IOT service integration、Cloud architecture、Automation processes、Regulatory Services、Clinical Services、Quality Services、Manufacturing Solutions和MDR
地点
Veranex员工
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Steve Maylish
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Jose Fernandez
Medical Device | Drug-Device Combination | Research and Development | Product Innovation | Vascular - Orthopedic - Laparoscopy - Energy - Minimally…
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Kim Rochat
Regulatory Enthusiast I Navigating Regulatory Challenges and Driving Creative Solutions
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Jurjen Zoethout
VP Regulatory & Quality | MedTech Consultancy at Veranex
动态
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How important is quality data? ?? VERY ?? Not only do AI algorithms rely on access to sound data, but it’s critical that data accurately reflects the population that it will be used in AND holds up to scrutiny so that we can continue to see positive health outcomes. Here’s what Michelle Tarver, MD, PhD had to say in her recent Medtech Pioneers podcast episode with guest host Jessica Richter. ?? Listen to the episode: https://lnkd.in/g4-vYdCW #Medtech #QualityCare #PatientSafety #HealthcareLeadership #Innovation Lisa Carmel, Jessica Richter, Michelle Tarver, MD, PhD, FDA
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Welcome to the Veranex Image of the Month! Today, you be the Anatomist! To which species does this image of an aortic arch (red arrow) belong? Share your response in the comments section below and let's discuss! https://hubs.la/Q02Z0R-40 #medicaldevices #innovation #comparativeanatomy #preclinicalresearch
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AI, AR, VR and surgical robotics on the horizon! Listen to our latest podcast episode featuring Lisa Carmel and Dr. Janani Reisenauer from Mayo Clinic to get in-depth insights on advances in tech on the bleeding edge of healthcare. Listen now ?? https://lnkd.in/g4-vYdCW #Surgery #AI #Medtech #RoboticSurgery #Innovation #MayoClinic
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Can you list of the ten key sections of a preclinical study final report? In our latest blog post, our team lays out what you need to include and best practices for including it so that reviewers can easily understand what you've submitted. Read the blog: https://hubs.la/Q02Yvb3Y0
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If you’re engaging in cardiac research or device development, our latest blog post from our preclinical team is a must read! We take a deep dive into: - The differences between ECMO and VAD in preclinical studies - Suitable vs. unsuitable models - Details on how procedures and studies are conducted - Potential challenges Read the blog post here ?? https://hubs.la/Q02Y9RC50 #ECMO #VAD #CardiacResearch #PreclinicalStudies #MedicalDevices #HealthcareInnovation
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Feeling confused or lost when it comes to navigating IVD regulations? Gain compliance confidence at our upcoming educational session in Lund, Sweden on November 26. You'll learn: - The ins and outs of new stringent regulatory constraints due to IVDR - Study design that will support high-quality clinical performance data - Plus, get a FREE IVDR check up with our team of experts! Register Now: https://hubs.la/Q02Y1PwH0
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Did you know that the FDA maintains a list of devices that use AI/ML? It's a great resource for companies that are looking for predicates and working to prove precedent for their device! ?? Listen to the episode: https://lnkd.in/g4-vYdCW #Medtech #QualityCare #PatientSafety #HealthcareLeadership #Innovation Lisa Carmel, Jessica Richter, Michelle Tarver, MD, PhD, FDA
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Need a break from work? How about a word search! Find three words related to integrated product development and comment below with what you found! Bonus points for sharing how you're incorporated them into your strategy! #IntegratedDevelopment #medtech #MedicalDevices #VeranexDevelops
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Navigating the complexities of biocompatibility is essential for ensuring safety and compliance in medtech product development. Join our online training on November 21 and 26 to deepen your knowledge and enhance your skills in this crucial area! In this 2-day course, you will: - Develop a foundational understanding of biocompatibility-related issues and requirements - Learn how to avoid costly mistakes when selecting materials - Gain insights to facilitate effective discussions on biological evaluations and much more! Whether you’re new to the field or looking to improve your expertise, this training is for you! Register now: https://hubs.la/Q02X6wXQ0 #Biocompatibility #MedTech #MedicalDevice #Training