Implications for Medtech Companies with FDA Rollout of the New QMSR to Replace Current QSR

Implications for Medtech

FDA issuance of the new Quality Management System Regulation (QMSR) to industry is meant to harmonize the current Quality System Regulation (QSR) for medical devices (21 CFR 820) with an incorporation by reference (IBR) to the 2016 edition of ISO 13485.

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OTHER ON-DEMAND WEBINARS

How to Tackle Medical Software Classification in 2022

During this webinar, we analyze medical product classification and software safety classification, provide an overview of the general requirements for IEC 60601-1 clause 14, the overlap with IEC 62304 and provide insights into the most common pitfalls.
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Purification Strategies for Industrial Antibody Manufacturing

Purification using chromatographic media and other methods is one of the most critical unit operations in the production of antibodies.
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Patient Engagement in Healthcare Increases ROI for the Marketing Budget

Sequence Health

Watch and learn how patient engagement in healthcare can significantly increase your leads and provide a positive return on your marketing spend for your Bariatric Program.
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Mediterranean Diet Extracts: The Clinical Benefit, Market Demand & Formulations

This webinar will introduce Mediterranean fruit and vegetables extracts, the context of the Mediterranean diet and healthy aging. Specifically, you’ll get insights on how the market is responding to a growing demand for premium
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