About
Join Nadège Krebs, PhD, Customer Consultant, Embase, Europe
Carlos Rodriguez del Rio, PhD, Product manager, Embase and learn more about:

• Standard literature searches:
• How to gather background information on guidelines or evidence-based-medicine for a disease or intended use.
• How to find clinical evidence data for a device in an intended use.
• How to compare devices for an intended use.
What if you cannot find literature because there is a gap ?
• The device is not mentioned, or the device’s existence is just assumed …ideas on how to quantitatively express a literature gap

Please keep in mind this webinar is not an explanation of the regulations, just a way of using tools to address an interpretation of the MDR guidelines.

At the end, you can request a short summary of a PICO search on your own device and we will send it to you.

Presenters
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Nadege Krebs
Customer Consultant for Embase.com
Nadège has a PhD in animal Sciences and after 10 years of selling and teaching about software in behavioral analysis for humans and animals, she joined Elsevier. For the past 3 years, she has been the dedicated Customer Consultant for Embase in Europe, managing over 100 accounts, onboarding new scientists with Embase, or doing customized and specific sessions for advanced users. With Covid, she focused on making trainings interactive despite the screen. She believes in ‘learning by doing’ and combing resources (Embase and PharmaPendium or Reaxys or Science Direct) to enhance the benefits of good literature searches.
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Carlos Rodriguez Del Rio
Product Manager Embase
Carlos holds a PhD in Chemistry and after years of research he joined Elsevier. Currently, he is the product manager of Embase, world's most comprehensive biomedical literature search solution. Before moving to the Embase product manager role, he worked as a Customer consultant. He is passionate about customer experience and is always determined on bringing new features into the Embase platform to make biomedical searches effortless for every user. He is also involved in many projects for improving the solution to transform it into the most effective platform for Medical Device development, pre-market approval and post-market surveillance.
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