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News and Resources

For Entrepreneurs

Medmarc supports Innovators who drive progress in life science technologies. Resources for Start-ups, R&D stage companies, and those preparing to Commercialize for the first time.

For Entrepreneurs

Medmarc supports Innovators who drive progress in life science technologies. Resources for Start-ups, R&D stage companies, and those preparing to Commercialize for the first time.

Adverse Event Reporting

Materials for life sciences companies wanting to know about tracking and reporting adverse events and information on the related regulatory and insurance duties.

Adverse Event Reporting

Materials for life sciences companies wanting to know about tracking and reporting adverse events and information on the related regulatory and insurance duties.

Clinical Trials

Resources for Companies conducting Human Clinical Trials: Informed Consents, Ethics and Institutional Review Boards, Introduction to Products Liability, Global Clinical Trials

Clinical Trials

Resources for Companies conducting Human Clinical Trials: Informed Consents, Ethics and Institutional Review Boards, Introduction to Products Liability, Global Clinical Trials

All Other Resources

Medmarc offers a variety of news and resources to provide in depth discussions regarding risk management and products liability issues in the life sciences industry

All Other Resources

Medmarc offers a variety of news and resources to provide in depth discussions regarding risk management and products liability issues in the life sciences industry

Upcoming Webinars

FDA Outlook: What to Expect in 2021

February 3, 2021

A look at potential changes facing FDA-regulated life sciences industry in 2021. Presented by James Boiani of Epstein Becker and Green.

Register

Recent Webinars

Claims 2020: A Year Unlike Any Other

Previously Recorded on December 16, 2020

In this year’s annual year-end wrap-up, a panel that includes members of Medmarc’s Claims team along...

Ripped From the Headlines: A(n Eventful) Year in Review

Previously Recorded on December 2, 2020

In this installment of Medmarc’s webinar series, Kate Klaus, an attorney and FDA specialist in our R...

The Potential Life Sciences Implications of the Election

Previously Recorded on October 28, 2020

The medtech industry has significantly changed during the Trump administration’s last four years. FD...

How to Write Effective and Compliant Standard Operating Procedures (SOPs)

Previously Recorded on September 1, 2020

In this session, presenter, Joy McElroy from McElroy Training and Consultancy, will discuss the bene...

Clinical Trials in The Era of COVID-19

Previously Recorded on June 17, 2020

This session presenters, Dianne Bourque and Benjamin Zegarelli from Mintz, will explore the widespre...

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