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Events

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Training
Biological Safety Training — January Course B
January 19, 2021 - January 20, 2021 All Day
Webinar
IVDR Implementation: First Steps for Compliance for Products Already on the European Market
January 21, 2021 11:00 AM - 12:00 PM ET
Training
Biological Safety Training — March Course A
March 23, 2021 - March 24, 2021
Training
Biological Safety Training — June Course A
June 8, 2021 - June 9, 2021 All Day
Training
Biological Safety Training — June Course B
June 15, 2021 - June 16, 2021 All Day
Webinar
Strategies for Selecting the Right In Vivo Models for Regulated Preclinical Studies
October 28, 2020
Webinar
Reimbursement Opportunities and Challenges in 2020: Factors for Success – A NAMSA and Kalms Consulting sponsored Q&A Panel Discussion
September 30, 2020
Webinar
Ensuring your Post-Market Surveillance Process Meets the New ISO 14971:2019 Guidance and MDR/IVDR Requirements
September 9, 2020
Webinar
Considerations for Clinical Study Start-Up in a Virtual Environment
August 19, 2020
Webinar
Achieving Medical Device Development Success Through Early Implementation of Regulatory, Reimbursement and Clinical Research Strategies
July 29, 2020
Webinar
Transitioning from EUA to 510(k) Clearance for IVD Products: What to Expect
July 16, 2020
Webinar
IVD Clinical Trials: Effective Site Selection Techniques - A Site and CRO Perspective
June 11, 2020
Webinar
EU MDR Part 2: How To Approach Clinical Evidence Requirements With Clinical Management & Biostatistics
June 3, 2020
Webinar
How to Manage Clinical Study Data During the COVID-19 Pandemic
May 13, 2020
Webinar
EU MDR Part 1: Current Opportunities & Challenges With Clinical Data-A NAMSA Panel Discussion
May 6, 2020
Webinar
Do’s & Don’t For Early-Stage IVD Product Development & Risk Mitigation
April 22, 2020
Webinar
Optimizing Electronic Data Capture (EDC) For IVD Clinical Trials
April 8, 2020
Webinar
The COVID-19 Pandemic: Proper Clinical Study Management & Protecting Data Validity
April 1, 2020
Webinar
The Value Of Biostatistics: Bringing A New Medical Device To Market
March 18, 2020
Webinar
4 Pillars Of IVDR: Integrating Post-Market Surveillance, Risk Management, QMS & Performance Evaluation
February 19, 2020
Webinar
The New ISO 10993-18:2020 – 10 Things Manufacturers Need To Know Today
February 4, 2020
Webinar
Design Control: Understanding the Benefits of Starting Early & Why It's Necessary
March 20, 2019
Webinar
Understanding Medical Device Reimbursement Fundamentals to Achieve Commercialization Success
February 20, 2019
Webinar
UNDERSTANDING AND APPLYING ISO 19227 REQUIREMENTS FOR ORTHOPEDICS MANUFACTURERS
January 17, 2019
Webinar
Understanding & Applying ISO 19227 Requirements for Orthopedics Manufacturers
January 17, 2019
Webinar
IVD Clinical Trials: Essential Components for Product Launch in 2019 & Beyond
November 6, 2018
Webinar
EU MDR: General Safety & Performance Requirements for the Biocompatibility of Medical Devices
October 23, 2018
Webinar
The New ISO 10993-1: 2018 – What Now?
August 27, 2018
Webinar
EU MDR 2017/745: Optimizing CERs within the Medical Device Lifecycle
August 7, 2018
Webinar
How to Effectively Navigate Radiation Sterilization Validation Scenarios
July 26, 2018
Webinar
Global Regulatory Requirements for Chemical Characterization: How to Cost-Effectively Demonstrate Biological Safety
July 12, 2018
Webinar
CFDA Acceptance of Overseas Clinical Trial Data: Understanding the Impact to Medical Device Manufacturers
April 20, 2018
Webinar
ISO 10993-1: Understanding the Use & Value of Biocompatibility Safety Evaluation & Risk Assessment Standards for Medical Devices
April 11, 2018
Webinar
Leveraging Post-Market Surveillance & Clinical Follow-Up Data to Support EU MDR Compliance
March 27, 2018

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