— Events —

join us at an upcoming event to learn direct from the experts

Region:

BIOMEDevice Boston

September 21, 2021 - September 22, 2021

Boston Convention Center, Boston

North American Biocompatibility Summit 2021

September 22, 2021 08:00 AM - 05:00 PM CT

Quincy Hall, Minneapolis

Pathology Assessment Of Medical Devices: Understanding the Basics

September 23, 2021 10:00 AM - 11:00 AM CT

American Association of Clinical Chemistry (AACC)

September 26, 2021 - September 30, 2021

Georgia World Congress Center, Atlanta, Georgia, Atlanta

The Medtech MVP

September 28, 2021 08:00 AM - 06:00 PM CT

Hilton Minneapolis, Minneapolis

Med-Tech Innovation Expo

September 28, 2021 - September 29, 2021

NEC, National Exhibition Centre, Birmingham

Meet with NAMSA at the MedTech Conference 2021

September 29, 2021 - September 30, 2021 All Day

Hyatt Regency Minneapolis, Minneapolis

Biological Safety Training—Amsterdam

October 4, 2021 - October 7, 2021 All Day

Kimpton De Witt Amsterdam, Amsterdam

Biological and Clinical Evaluations Conference for Medical Devices

October 5, 2021 - October 6, 2021

Sankt Gertrud Conference, Malmö

La Rentrée du DM

October 6, 2021 - October 7, 2021 All Day

Le Grand Kursaal, Besançon

Medical Technology Ireland

October 20, 2021 - October 21, 2021

Galway Racecourse, Galway

Symposium on Advanced Wound Care

October 29, 2021 - October 31, 2021

Caesars Palace Las Vegas, Las Vegas

MD&M Minneapolis

November 3, 2021 - November 4, 2021

Minneapolis Convention Center, Minneapolis

MEDICA

November 15, 2021 - November 18, 2021 All Day

Messe Dusseldorf, Dusseldorf

ISO 10993-18:2020 Chemical Characterization Of Materials Workshop— Frankfurt

November 23, 2021 09:00 AM - 03:45 PM GMT

Fleming’s Conference Hotel Frankfurt, Frankfurt am-Main

ASCA Accreditation for Biocompatiblity Testing: What’s it All About?

August 25, 2021

Analysis Of Medical Claims Data For Economic Summaries And Alternative Uses

The Critical Role of Biostatistics in Streamlining the Preclinical to Clinical Pathway

Alternative Test Methods for Medical Device Sterilization Validation: An Industry Panel Discussion

SaMD Product Development: Addressing Challenges through Early Integration of Regulatory, Quality and Clinical Data Strategies

Key Factors for Successful Clinical Study Database Design and Data Management

MDR Clinical Evaluation Reports: Key Elements and Lessons Learned for Successful Compliance

February 25, 2021

ISO 10993-23:2021 Tests For Irritation – What Manufacturers Must Understand Today

February 3, 2021

IVDR Implementation: First Steps for Compliance for Products Already on the European Market

January 21, 2021

Strategies for Selecting the Right In Vivo Models for Regulated Preclinical Studies

October 28, 2020

Reimbursement Opportunities and Challenges in 2020: Factors for Success – A NAMSA and Kalms Consulting sponsored Q&A Panel Discussion

September 30, 2020

Ensuring your Post-Market Surveillance Process Meets the New ISO 14971:2019 Guidance and MDR/IVDR Requirements

September 9, 2020

Considerations for Clinical Study Start-Up in a Virtual Environment

August 19, 2020

Achieving Medical Device Development Success Through Early Implementation of Regulatory, Reimbursement and Clinical Research Strategies

Transitioning from EUA to 510(k) Clearance for IVD Products: What to Expect

IVD Clinical Trials: Effective Site Selection Techniques - A Site and CRO Perspective

EU MDR Part 2: How To Approach Clinical Evidence Requirements With Clinical Management & Biostatistics

How to Manage Clinical Study Data During the COVID-19 Pandemic

EU MDR Part 1: Current Opportunities & Challenges With Clinical Data-A NAMSA Panel Discussion

Do’s & Don’ts For Early-Stage IVD Product Development & Risk Mitigation

Optimizing Electronic Data Capture (EDC) For IVD Clinical Trials

The COVID-19 Pandemic: Proper Clinical Study Management & Protecting Data Validity

The Value Of Biostatistics: Bringing A New Medical Device To Market

4 Pillars Of IVDR: Integrating Post-Market Surveillance, Risk Management, QMS & Performance Evaluation

February 19, 2020

The New ISO 10993-18:2020 – 10 Things Manufacturers Need To Know Today

February 4, 2020

Design Control: Understanding the Benefits of Starting Early & Why It's Necessary

Understanding Medical Device Reimbursement Fundamentals to Achieve Commercialization Success

February 20, 2019

UNDERSTANDING AND APPLYING ISO 19227 REQUIREMENTS FOR ORTHOPEDICS MANUFACTURERS

January 17, 2019

Understanding & Applying ISO 19227 Requirements for Orthopedics Manufacturers

January 17, 2019

IVD Clinical Trials: Essential Components for Product Launch in 2019 & Beyond

November 6, 2018

EU MDR: General Safety & Performance Requirements for the Biocompatibility of Medical Devices

October 23, 2018

The New ISO 10993-1: 2018 – What Now?

August 27, 2018

EU MDR 2017/745: Optimizing CERs within the Medical Device Lifecycle

How to Effectively Navigate Radiation Sterilization Validation Scenarios

Global Regulatory Requirements for Chemical Characterization: How to Cost-Effectively Demonstrate Biological Safety

CFDA Acceptance of Overseas Clinical Trial Data: Understanding the Impact to Medical Device Manufacturers

ISO 10993-1: Understanding the Use & Value of Biocompatibility Safety Evaluation & Risk Assessment Standards for Medical Devices

Leveraging Post-Market Surveillance & Clinical Follow-Up Data to Support EU MDR Compliance

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