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.

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

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

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.

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

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

A Strategic Roadmap: Assessing Safety & Biocompatibility of Medical Devices

November 21, 2019

The regulatory landscape for the safety evaluation, clinical testing and commercial development of medical devices is undergoing considerable changes, including new requirements for material characterization and chemical risk assessment early on in the development process. In this webinar, toxicolog...

Recent Webinars

Ripped from the Headlines: Medmarc’s Risk Management Team Discusses Top Stories in Life Sciences

Previously Recorded on October 22, 2019

The life sciences landscape is constantly—and rapidly—evolving. Staying on top of news and trends is...

United States: DOJ's New Corporate Compliance Evaluation Guidance and the Potential Impact on Life Sciences Companies

Previously Recorded on September 18, 2019

Earlier this year, the Criminal Division of the U.S. Department of Justice (DOJ) issued updated guid...

The Current State of Cybersecurity in Medical Devices

Previously Recorded on August 22, 2019

As medical devices become more connected and interactive with health care providers and patients, fu...

3D Printing of Medical Devices: What the Future Holds for Regulating and Litigating Medical Device Failures for Point of Service Manufacturers and Users

Previously Recorded on July 24, 2019

3D printing has been a disruptive technology to the medical device industry, and its use and applica...

Current Regulatory and Litigation Developments in the 510(k) Process: Everything You Need to Know and More

Previously Recorded on June 27, 2019

The 510(k) process has been the subject of recent media attention as well as litigation. Many have a...

News and Resources

For Entrepreneurs

Adverse Event Reporting

Clinical Trials

All Other Resources

For Entrepreneurs

Adverse Event Reporting

Clinical Trials

All Other Resources

For Entrepreneurs

For Entrepreneurs

Adverse Event Reporting

Adverse Event Reporting

Clinical Trials

Clinical Trials

All Other Resources

All Other Resources

Upcoming Webinars

Recent Webinars

Featured Videos