Jacqueline van Druten (MICR.CIM.RD)的动态

What does a compliant systematic literature review for medical devices look like? From screening for bias to levels of evidence, get access to rich insights within this recorded webinar and other resources on medical device regulation. https://spkl.io/6048f8zBp #EUMDR #MedicalDevices

The Medical Device Regulation: Why is there a need for clinical expert involvement in developing new medical devices? In this guest blog from Esther Daemen, we look at the need for the involvement of clinical experts in developing new medical devices, from concept to completion, and the importance of adhering to the new Medical Device Regulation (MDR). More: https://lnkd.in/eisRjFuT #gcpcentral #thereisabetterway #medicaldevices #clinicalresearch #experts

Gain a breakdown of why post-market clinical follow-up (PMCF) is crucial for medical device regulation and how it can be tailored for different devices in our latest feature >>> https://hubs.ly/Q02KzS1f0

?? How much does medical device testing cost? We always get this question, and answering it isn't straightforward. The response most of the time is - it depends. Discover the top 5 key considerations when evaluating the cost of medical device testing. Learn more: https://lnkd.in/ehPQcAP3 #medicaldevices #mdr #fda

** Newest Blog Post ** Top 5 Regulatory Trends in the Advanced Medical Device Industry A Link to the Article: https://lnkd.in/gfgMgstn

There are about 2 million medical devices on the market today, and each of them underwent a journey from innovation through clinical trials to the market. The journey might look familiar, but medical device trials come with particular challenges. Here we look at what they are and how to overcome them. https://buff.ly/3LZePS0 #MedicalDevice #ClinicalTrials #ClinicalResearch

?? Exciting News! ?? We've just released the latest "Guiding Principles for Medical Device Registration Review" (2023 Edition)! ?? This comprehensive catalog is a game-changer for the medical device industry, enhancing scientific review capabilities and fostering high-quality development. ?? Perfect for professionals and enthusiasts alike. ???? Dive into the depths of these principles and see how they can revolutionize your approach to medical device registration. ?? We welcome all inquiries - reach out to [email protected] for more info #MedicalDeviceInnovation

Industry Spotlight: Medical Device Manufacturing The use of permanent marks in the medical industry is critical to ensure the safety of operators and patients. Learn more: https://buff.ly/3Vm2Pi0

Practical Approaches for Sound Medical Device Development https://buff.ly/3wjYodG

New Blog: "The Path to Launching a Medical Device in the USA: A Guide by OneGlobal Trinity M Consulting." Read more below. https://wix.to/QbUicbZ #trinitymconsulting #globalconsulting #medicaldevices #newblogpost