Virtual health: What's on the horizon for telehealth and remote monitoring?

As the world responds to the COVID-19 pandemic, physicians and patients are increasingly turning to virtual health solutions, including telehealth and remote monitoring, as a central facet...

Paths for medical device companies to partner with the federal government

Tapping into the federal market in the COVID-19 environment

How COVID-19 is changing the clinical trials landscape

Among the numerous repercussions of the COVID-19 pandemic, life sciences companies and academic medical centers are now faced with significant disruptions and threats to their clinical...

EU MDR: Quality System Alignment Conference

Dennis C. Gucciardo and Fabien Roy spoke at Q1 Productions' EU MDR: Quality System Alignment Conference in Chicago, Illinois on 4 December 2019.

Webinar: Understanding the FDA – Accelerating the Pathway to Approval for Point-of-Care Technologies

Senior director Susan D. Tiedy-Stevenson was a featured speaker for the webinar titled "Understanding the FDA – Accelerating the Pathway to Approval for Point-of-Care Technologies"...

Sydney: Join leaders from Hogan Lovells Medical Device team for conversation and cocktails

We welcome you to join members of our medical device and health care regulatory team as we discuss how to navigate the shifting regulatory landscape facing medical device firms. From...

9th Annual Medical Device Supplier Quality Assurance Conference

Dennis Gucciardo addressed the regulatory clarification on risk assessment within the ISO 13485:2016 framework at the 9th Annual Medical Device Supplier Quality Assurance Conference.

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