Informed Consent
Human Subject Protection in the Digital Health Age


Tuesday, March 31, 2020 • 1:30 p.m. - 3:00 p.m. EDT

NEW: The webinar will be updated to include last week’s guidance from the FDA on conducting clinical trials during the COVID-19 pandemic, including how to determine when changes need to be made to the protocol and consent forms.


Digital technologies that collect personal healthcare information are a blessing for clinical trial specialists.

It’s helpful to have the medical info for research purposes, but you need a solid understanding of the latest FDA and federal regulations for informed consent and human subject protection.

Join CenterWatch and experts Michael Werner and Sara Klock for a comprehensive webinar on how to comply with FDA and other federal regulation of digital technologies March 31.

Webinar Takeaways:

  • Assess how digital technologies used to gather, analyze and report healthcare data for medical treatment purposes or to promote a healthy lifestyle can also be used for research purposes
  • Familiarize yourself with the regulatory landscape to understand how digital technologies and the information they gather and use in research will be regulated
  • Determine how to design clinical trials using digital technologies that comply with the 21st Century Cures Act and changes to the Common Rule
  • Identify what activities can be undertaken to develop new digital technologies without triggering federal research regulations
  • Find out how to develop informed consent forms when Institutional Review Board oversight is required, and other compliance questions
  • Identify factors likely to determine whether and to what extent certain technologies are regulated as medical devices by FDA

In the era of digital information collection you need to know how to gather, analyze and report healthcare data that is obtained electronically. Join us by registering today.

Who Will Benefit

  • M&A groups focusing investment in the medical device or health IT space
  • Medical device companies
  • Pharmaceutical and biotechnology companies
  • Developers and marketers of digital technology related to disease, health, fitness or a healthy lifestyle
  • Legal counsel, technology developers and investors
  • Regulatory affairs/compliance professionals
  • Medical professionals
  • Quality professionals
  • Clinical trials professionals
  • Digital health professionals

Webinar plus USB Audio Recording/Transcript
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$487

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Webinar only
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$287

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24/7 Encore plus USB Audio Recording/Transcript
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$487

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24/7 Encore Presentation
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$287

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USB Audio Recording/Transcript
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$287

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Meet Your Presenters

Michael Werner

Public Policy and Regulatory Attorney
and Co-leader
Holland & Knight's Healthcare & Life Sciences Team

Michael Werner is a Washington, D.C., public policy and regulatory attorney and a co-leader of Holland & Knight's Healthcare & Life Sciences Team. Mr. Werner has almost three decades of healthcare law, lobbying, regulatory, and reimbursement experience in D.C. He focuses on issues affecting FDA-regulated entities, including medical device, biotechnology and pharmaceutical companies developing and manufacturing prescription and over-the-counter (OTC) drugs, biosimilars, cosmetics, dietary supplements, and digital-health technologies.

Sara Klock

Attorney and Member
Holland & Knight's Public Policy & Regulation Group

Sara Klock is a Washington, D.C., attorney and a member of Holland & Knight's Public Policy & Regulation Group. Ms. Klock focuses her practice on food, drug and device, life sciences, and political law. She advises life sciences clients on regulatory matters before federal and state agencies and law enforcement authorities, including the U.S. Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Federal Trade Commission (FTC), as well as the Food, Drug, and Cosmetic Act (FDCA) and the Controlled Substances Act (CSA).