In this on-demand webinar, delve into pragmatic approaches for clinical evidence generation and regulatory acceptance. This discussion examines recent FDA draft guidance on integrating RWD/RWE in medical device studies and explores case studies of companies effectively leveraging RWE. https://lnkd.in/eu5c3T5P Presenters: Craig Serra, Flatiron Health Josh Buddle, Flatiron Health Jonathan Helfgott, The Johns Hopkins University Tara Marti, Exact Sciences
Clinical Tech Leader的动态
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Staying Ahead with Medical Innovations ? While leading in clinical trials, 3SYNC Research is also keenly aware of emerging medical breakthroughs, such as the new AI-generated COVID drug now entering Phase I trials. Promising to be effective against all variants, this oral medication could soon offer a significant alternative to current treatments. It's a testament to our commitment to staying at the forefront of healthcare advancements. Learn more about this promising development here: 3sync.com 1-800-733-7962 #MedicalInnovation #COVID19Research #3SYNCResearch
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How can we unlock the potential of digitizing clinical trials, accelerating research and improving the experience for patients and sites? In collaboration with Transcelerate, my colleague Kelsey Jakee sheds light on the incremental steps companies can take to bring about positive change #ClinicalTrials #DigitalTransformation #PharmaInnovation
Digitizing the clinical protocol: Small steps for seismic change
paconsulting.smh.re
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?? New Blog Post: FDA Guidance on Diversity in Clinical Trials Discover how the FDA's guidance is paving the way for more inclusive and representative clinical trials. Our latest post explores key strategies and the importance of diversity in clinical research. ?? Read the full blog post here: https://bit.ly/3x2Y7vY
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Innovative Business Development Manager | 13+ Years in Clinical Trials | Diversity Advocate | Disrupting the Industry Status Quo | CRIO Employee, Opinions my own
Hi everyone! This is a blog post you do not want to miss! It is a comprehensive view of the FDA guidance focused on trial design approaches like flexible visit windows and use of digital health technologies. What do you think is coming next from the FDA about diversity? #inclusiveclinicaltrials #clinicalresearch #clinicaltrials
?? New Blog Post: FDA Guidance on Diversity in Clinical Trials Discover how the FDA's guidance is paving the way for more inclusive and representative clinical trials. Our latest post explores key strategies and the importance of diversity in clinical research. ?? Read the full blog post here: https://bit.ly/3x2Y7vY
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Let's re-think how we target and recruit patients ?? Let's re-think how we keep patients enrolled in clinical trials ?? #diversity #clinicaltrials #clinicalresearch
?? New Blog Post: FDA Guidance on Diversity in Clinical Trials Discover how the FDA's guidance is paving the way for more inclusive and representative clinical trials. Our latest post explores key strategies and the importance of diversity in clinical research. ?? Read the full blog post here: https://bit.ly/3x2Y7vY
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Check out this blog post I co-wrote with Marc Wartenberger!
?? New Blog Post: FDA Guidance on Diversity in Clinical Trials Discover how the FDA's guidance is paving the way for more inclusive and representative clinical trials. Our latest post explores key strategies and the importance of diversity in clinical research. ?? Read the full blog post here: https://bit.ly/3x2Y7vY
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Sr Bio-Pharmaceutical Executive | General Management | US & Global | Marketing & Sales | Syneos Health/Pacira BioPharmaceuticals/AstraZeneca
Bridging the gap between Drug Development and then getting the medicine into the hands of patients.... Our experts Amanda Bruno and Angela Wlodar explore how medical science liaisons (MSLs) bridge the gap between R&D teams and commercial teams, the challenges in quantifying MSLs value, how their role is expanding and more. Learn more in their PM360 article: https://ow.ly/bCaF30sBZU0 #SyneosHealth
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Wondering why your CRO is suggesting an adaptive clinical trial? As the name suggests, an adaptive design allows for more flexibility, which can be especially useful if there are uncertainties specific to your drug. Being able to change the course of your study as data accumulates means getting crucial answers sooner—saving you both time and money. Dr. Gaetano Morelli, Chief Medical Officer, shares more insight on adaptive clinical trials at Altasciences. #WeAreAltasciences #DrugDevlopment #ClinicalResearch
Ask an Altascientist | Adaptive Clinical Trials
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Clinical-translational studies are essential in the validation of medical and diagnostic devices. These studies are pivotal in transitioning diagnostic technologies from the laboratory to clinical practice. By evaluating diagnostic accuracy, clinical utility, and compliance with regulatory guidelines, these studies ensure that new diagnostic tools are effective and reliable in real-world settings. Discover how clinical-translational studies contribute to advancing medical diagnostics and improving patient outcomes in our blog post. Read more here: https://lnkd.in/eFke85nf #ClinicalResearch #DiagnosticDevices #Biostatistics #HealthcareInnovation #AnatomiseBiostats #ClinicalTranslationalStudies
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Digitising clinical trials has the potential to accelerate clinical research and improve patient and site experience. But with many digitisation efforts in healthcare, how do you do it without further worsening the digital divide? My colleague, Kelsey Jakee, alongside Transcelerate, explains how companies can take small steps to realise positive change. #ClinicalTrials #DCTs #DecentralizedTrials #PharmaInnovation
Digitizing the clinical protocol: Small steps for seismic change
paconsulting.smh.re
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