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

Guiding Light – How Codes of Ethics Mitigate Risk and Elevate the Industry

November 16, 2018

***This webinar has been rescheduled to November 16th.*** Ethical conduct is critical in all business operations, but especially so in industries like life sciences, where health and safety are at stake. Codes of ethics can serve as a statement to outside stakeholders and policymakers about the ty...

Recent Webinars

Grants or Startup Tax Credit - Which one is right for you?

Previously Recorded on September 19, 2018

For life science startups, two of the primary sources of non-dilutive funding are Grants and the Pay...

Crisis Management When the Big Case Hits: How to Get Ready and What to Do When the Alarm Is Sounded

Previously Recorded on August 30, 2018

Even the safest products may be the subject of products liability lawsuits at some point, and compan...

Keys to an Effective Complaint-Handling System: How to Audit and Improve Yours

Previously Recorded on July 18, 2018

In this webinar, seasoned regulatory attorney Edward C. Wilson, Jr., Partner at Hogan Lovells’ Washi...

My Product Is on the Market; Now What?

Previously Recorded on June 27, 2018

The design is complete. The label is finalized. The product is approved and sold. But the risks of l...

Big Legislative Changes: What You Need to Know to Meet the New Compliance Challenges

Previously Recorded on May 29, 2018

Two new major pieces of legislation – the Food and Drug Administration Reauthorization Act (FDARA) 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

Risk Management Video Series