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Press Release
Nov 28, 2018
State of the Art Literature Review for EU MDR Compliance: How to Get It Right, New Webinar Hosted by Xtalks
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Press Release
Nov 21, 2018
5 Signs You Need to Re-Evaluate Your Clinical Trial Management and Simple Steps to Improve Efficiency, New Webinar Hosted by Xtalks
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Press Release
Nov 21, 2018
Simplifying Clinical Data Flow From EDC to SDTM, New Webinar Hosted by Xtalks
5 lessons to master clinical data aggregation, transformation, cleaning and analytics to reduce cost, risk and time
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Press Release
Nov 21, 2018
How to Develop a Global Clinical Study Budget Like a Pro, New Webinar Hosted by Xtalks
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Press Release
Nov 1, 2018
Assembling the eClinical Suite: Taking Advantage of the Latest Technology While Avoiding Vendor Lock-Ins, New Webinar Hosted by Xtalks
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Press Release
Oct 30, 2018
Medical Device Development: Using Advanced Simulation Technologies and Computer-Aided Engineering to Accelerate Time to Market, New Webinar Hosted by Xtalks
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Press Release
Oct 22, 2018
5 Critical Questions Small to Mid-Sized Sponsors Need to Ask When Evaluating an EDC Provider, New Webinar Hosted by Xtalks
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Press Release
Oct 16, 2018
Pfizer and Bracket - How to Apply Patient-Centric Concepts to All Stages of Clinical Trials, New Webinar Hosted by Xtalks
Much of the discussion around patient-centricity today is centered around trial design, which is important and commendable work. Unfortunately, focusing primarily on design overlooks how to instill patient-centric concepts and create a friendly environment in the study once the protocol is finalized.
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Press Release
Aug 24, 2018
How to Ensure Compliance With the New EU Medical Device Regulations: MDR & IVDR, New Webinar Hosted by Xtalks
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Press Release
Mar 15, 2018
FDA Perspectives on Computer Simulations in the Evaluation of Medical Devices, New Webinar Hosted by Xtalks
Live discussion with FDA and Siemens to provide an overview of the use of individualized computer simulation to predict clinical outcomes in medical device trials
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