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Events

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Webinar
Transitioning from EUA to 510(k) Clearance for IVD Products: What to Expect
July 16, 2020 11:00 AM - 12:00 PM
Webinar
Achieving Medical Device Development Success Through Early Implementation of Regulatory, Reimbursement and Clinical Research Strategies
July 29, 2020 10:00 AM - 11:00 AM
Tradeshow
Extractables and Leachables Virtual Summit 2020
July 30, 2020 - July 31, 2020
Tradeshow
MEDI’NOV Connection 2020
September 9, 2020 - September 10, 2020 All Day
Matmut Stadium de Gerland, Lyon
Tradeshow
Med-Tech Innovation Expo
September 29, 2020 - September 30, 2020
NEC, National Exhibition Centre, Birmingham
Training
Biological Safety Training—Amsterdam
October 5, 2020 - October 8, 2020 All Day
Kimpton De Witt Amsterdam, Amsterdam
Training
ISO 10993-18:2020 Chemical Characterization Of Materials Workshop—Frankfurt
November 18, 2020 09:00 AM - 04:30 PM CET
Fleming’s Conference Hotel Frankfurt, Frankfurt am-Main
Webinar
IVD Clinical Trials: Effective Site Selection Techniques - A Site and CRO Perspective
On Demand
Webinar
Leveraging Post-Market Surveillance & Clinical Follow-Up Data to Support EU MDR Compliance
On Demand
Webinar
How to Manage Clinical Study Data During the COVID-19 Pandemic
On Demand
Webinar
EU MDR Part 2: How To Approach Clinical Evidence Requirements With Clinical Management & Biostatistics
On Demand
Webinar
EU MDR Part 1: Current Opportunities & Challenges With Clinical Data-A NAMSA Panel Discussion
On Demand
Webinar
Do’s & Don’t For Early-Stage IVD Product Development & Risk Mitigation
On Demand
Webinar
Optimizing Electronic Data Capture (EDC) For IVD Clinical Trials
On Demand
Webinar
The COVID-19 Pandemic: Proper Clinical Study Management & Protecting Data Validity
On Demand
Webinar
The Value Of Biostatistics: Bringing A New Medical Device To Market
On Demand
Webinar
4 Pillars Of IVDR: Integrating Post-Market Surveillance, Risk Management, QMS & Performance Evaluation
On Demand
Webinar
The New ISO 10993-18:2020 – 10 Things Manufacturers Need To Know Today
On Demand
Webinar
Design Control: Understanding the Benefits of Starting Early & Why It's Necessary
On Demand
Webinar
Understanding Medical Device Reimbursement Fundamentals to Achieve Commercialization Success
On Demand
Webinar
UNDERSTANDING AND APPLYING ISO 19227 REQUIREMENTS FOR ORTHOPEDICS MANUFACTURERS
On Demand
Webinar
Understanding & Applying ISO 19227 Requirements for Orthopedics Manufacturers
On Demand
Webinar
IVD Clinical Trials: Essential Components for Product Launch in 2019 & Beyond
On Demand
Webinar
EU MDR: General Safety & Performance Requirements for the Biocompatibility of Medical Devices
On Demand
Webinar
The New ISO 10993-1: 2018 – What Now?
On Demand
Webinar
EU MDR 2017/745: Optimizing CERs within the Medical Device Lifecycle
On Demand
Webinar
How to Effectively Navigate Radiation Sterilization Validation Scenarios
On Demand
Webinar
Global Regulatory Requirements for Chemical Characterization: How to Cost-Effectively Demonstrate Biological Safety
On Demand
Webinar
CFDA Acceptance of Overseas Clinical Trial Data: Understanding the Impact to Medical Device Manufacturers
On Demand
Webinar
ISO 10993-1: Understanding the Use & Value of Biocompatibility Safety Evaluation & Risk Assessment Standards for Medical Devices
On Demand

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