Bridging the GAP Agile/Compliance

Bridging the gap between agile and compliance is a hard task. Join this webinar to gain a better understanding on how your R&D, QA and Compliance teams can work better together.

Bridging the gap between agile and compliance is a hard task. Join this webinar to gain a better understanding on how your R&D, QA and Compliance teams can work better together.

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Crossing the eSTAR Chasm: Transitioning to FDA’s Mandatory 510k eSTAR Submission Process by October 2023

This webinar will educate and prepare medical device manufacturers, regulatory affairs leaders, and regulatory consultants to effectively transition their processes, resources, and operations to seamlessly adopt the eSTAR as the new submission standard. This session will share watchouts, best practices, and tips and tricks to adapt to eSTAR.

This webinar will educate and prepare medical device manufacturers, regulatory affairs leaders, and regulatory consultants to effectively transition their processes, resources, and operations to seamlessly adopt the eSTAR as the new submission standard. This session will share watchouts, best practices, and tips and tricks to adapt to eSTAR.

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Accelerating Corrective Actions for Rapid Introduction of New Products: Strategies for Success

Join us as we explore strategies to accelerate corrective actions and streamline the introduction of new products. Our esteemed panel of industry experts will share their perspectives, experiences, and best practices in navigating these critical business challenges.

Join us as we explore strategies to accelerate corrective actions and streamline the introduction of new products. Our esteemed panel of industry experts will share their perspectives, experiences, and best practices in navigating these critical business challenges.

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Not All Medical Products Are Created Equal. Harnessing the Power PLM!

Learn how PLM helps medical device companies make informed decisions about when to invest in new product development, when to retire existing products, and how to align to evolving customer requirements, leading to a more successful and sustainable product strategy.

Learn how PLM helps medical device companies make informed decisions about when to invest in new product development, when to retire existing products, and how to align to evolving customer requirements, leading to a more successful and sustainable product strategy.

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Mastering EU MDR: Essential Strategies for Effective Risk and Document Management

Risk & Document management is an essential part of the MDR process. Join this webinar to gain a better understanding of the risk management process, key requirements of MDR and best practices for compliance.

Risk & Document management is an essential part of the MDR process. Join this webinar to gain a better understanding of the risk management process, key requirements of MDR and best practices for compliance.

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Defend Against MedTech Cyber Breach: A Fireside Chat with Critical Healthcare Stakeholders

What is your role in keeping patients safe, securing data privacy, and reducing potential liability from cyber breach through the connected devices you prescribe, design, or distribute? Join security leaders from Partners Healthcare, GE Healthcare, Zipnosis, and Irdeto for a discussion of point-of-care-wide best practices and current technology solutions to defend against potential risks and dangers to your patients and your organization.

What is your role in keeping patients safe, securing data privacy, and reducing potential liability from cyber breach through the connected devices you prescribe, design, or distribute? Join security leaders from Partners Healthcare, GE Healthcare, Zipnosis, and Irdeto for a discussion of point-of-care-wide best practices and current technology solutions to defend against potential risks and dangers to your patients and your organization.

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