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Tradeshow
Extractables & Leachables Summit 2023
April 17, 2023 - April 18, 2023 All Day
Wyndham Philadelphia Historic District, Philadelphia
Tradeshow
Design of Medical Devices Conference 2023
April 18, 2023 - April 19, 2023 All Day
Graduate Minneapolis, Minneapolis
Webinar
Telling Your Medical Device's Story to Regulatory Agencies
April 19, 2023 10:00 AM - 11:00 AM CT
Training
Biological Safety Training—Tokyo
April 24, 2023 - April 26, 2023 All Day
Nihonbashi Life Science HUB, Chuo-Ku, Tokyo
Tradeshow
Smithers' Extractables & Leachables USA 2023
May 17, 2023 - May 18, 2023 All Day
The Westin Arlington Gateway, Arlington
Training
Biological Safety Training — Virtual Course A
June 13, 2023 - June 14, 2023 All Day
Training
Biological Safety Training — Virtual Course B
June 20, 2023 - June 21, 2023 All Day
Training
ISO 10993-18:2020 Chemical Characterization Of Materials Workshop— Virtual
June 27, 2023 09:00 AM - 03:45 PM CET
Training
Biological Safety Training—Lyon
September 18, 2023 - September 21, 2023 All Day
Sofitel Lyon Bellecour, Lyon
Training
Biological Safety Training—Philadelphia
October 9, 2023 - October 12, 2023 All Day
Kimpton Hotel Palomar Philadelphia, Philadelphia
Webinar
Clinical Trial Site Budgeting – Risk Mitigation or Budget Control?
March 16, 2023
Webinar
A Practical Guide to Writing Summaries of Safety and Clinical Performance
March 14, 2023
Webinar
Navigating Trends and Best Practices for Cardiovascular Device Development
February 22, 2023
Webinar
Exhaustive Extractions in E&L Studies – Endpoint Determination Challenges, Expectations and Reality
January 11, 2023
Webinar
Navigating the Landscape for Over-the-Counter or Direct-to-Consumer IVD Tests
December 8, 2022
Webinar
Optimizing Preclinical Testing for Cardiovascular Medical Devices
October 13, 2022
Webinar
Biostatistics in IVD Clinical Research – Decoding the Biostatistical Black Box
September 22, 2022
Webinar
Chemical Characterization Best Practices: Assumptions of TTC and Exhaustive Extraction
August 24, 2022
Webinar
FDA QMSR: What do the Proposed Changes Mean for Industry?
August 3, 2022
Webinar
FDA and NAMSA Present: Reducing Regulatory Burden and Streamlining FDA Review through ASCA Pilot Program Utilization
July 20, 2022
Webinar
ISO 14155:2020 – What Every Clinical Professional Should Know
June 30, 2022
Webinar
The Basics of IVDR Clinical Studies
May 26, 2022
Webinar
Transitioning from EUA to 510(k) for IVD Products: Planning to Execution
April 21, 2022
Webinar
Clinical Challenges under the EU MDR
March 24, 2022
Webinar
Pathology Assessment Of Medical Devices: Understanding the Basics
September 23, 2021
Webinar
ASCA Accreditation for Biocompatiblity Testing: What’s it All About?
August 25, 2021
Webinar
Analysis Of Medical Claims Data For Economic Summaries And Alternative Uses
July 15, 2021
Webinar
The Critical Role of Biostatistics in Streamlining the Preclinical to Clinical Pathway
June 16, 2021
Webinar
Alternative Test Methods for Medical Device Sterilization Validation: An Industry Panel Discussion
May 20, 2021
Webinar
SaMD Product Development: Addressing Challenges through Early Integration of Regulatory, Quality and Clinical Data Strategies
April 21, 2021
Webinar
Key Factors for Successful Clinical Study Database Design and Data Management
March 18, 2021
Webinar
MDR Clinical Evaluation Reports: Key Elements and Lessons Learned for Successful Compliance
February 25, 2021
Webinar
ISO 10993-23:2021 Tests For Irritation – What Manufacturers Must Understand Today
February 3, 2021
Webinar
IVDR Implementation: First Steps for Compliance for Products Already on the European Market
January 21, 2021
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’ts 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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