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12-16 October 2020
★ VIRTUAL EVENT
Delivered in CEST Time Zone
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I'm speaking at MedTech Summit!
Use VIP Code MTCHVJOINME10 to save 10% off* your pass
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Carlos Rodriguez Delrio
Elsevier
Talk Title
Streamlining the Post-Market Surveillance Planning for Biomedical Literature, Tuesday, 13th October at 15:55 PM CET / 9:45 AM EDT
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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BRINGING THE LATEST EU MDR, IVDR AND GLOBAL MARKET REGULATORY GUIDANCE TO YOU
Join the European Commission, Competent Authorities, Notified Bodies and industry online for the answers you need to accelerate your path to compliance
Get the same dedicated coverage of PMS & Vigilance, Clinical Strategies, Combination Products, Software, Law, Biocompatibility and Medical Device Regulatory Project Management from the comfort of your own seat
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MEDTECH SUMMIT VIRTUAL AGENDA AT A GLANCE
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Plus, an online Medical Device Regulatory Project Management training course spread across 4 days at
14:00 – 17:00, on 27-30 October.
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PUT YOUR QUESTIONS DIRECTLY TO COMPETENT AUTHORITIES, NOTIFIED BODIES AND INDUSTRY INCLUDING
Gavia Taan
Unit Manager – Devices Regulatory Policy Devices Division
MHRA
Augusto Geyer
Deputy General Manager, Medical Devices Office
ANVISA, Brazil
Elaine Darcy
European Medical Device Operations Manager
NSAI
Daniele Bollati
Product Conformity Assessment /Medical Devices Expert
IMQ
Katharina Gruchenberg
Team Leader Biocompatibility and Materials of Animal Origin
TÜV SÜD Product Service GmbH
Erik Vollebregt
Partner
Axon Lawyers, The Netherlands
Alexandra Stamati
Director, Quality Assurance-PRRC
Medicon Hellas SA
Maham Ansari
Director of Regulatory Affairs
Synaptive Medical, Canada
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TIME'S RUNNING OUT. JOIN US TO GET YOUR QUESTIONS ANSWERED...
Connect with your fellow industry professionals online this October to benchmark, be inspired and prepare to meet the fast approaching compliance deadlines.
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*Use VIP code MTCHVJOINME10 to get 10% off*
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*1) Discounts not applicable to supplier/vendor/consultant/solution provider companies. Informa Connect Life Sciences will verify whether you are a supplier/vendor/consultant/solution provider when your registration is processed. 2) Discounts not to be used in conjunction with any other discount. 3) Discount not applicable to existing bookings.