Skip to main content

Webinar | Intellectual Property Issues in Clinical Trials

Thank you

This live web event has ended. Thank you for attending.

Description

Essential Components of a Clinical Trial Agreement | Webinar Series

Clinical trials are essential for developing new drugs and medical devices that can improve health outcomes and quality of life. However, they also involve complex intellectual property issues that can affect the rights and interests of the parties involved, such as sponsors, investigators, institutions, participants, regulators, competitors, and the public. This webinar will provide a comprehensive overview of the intellectual property issues in clinical trials.

Learning Objectives:

  1. Learn strategies and challenges protecting and commercializing intellectual property in clinical trials.
  2. Learn the roles and responsibilities of the parties involved in managing intellectual property in clinical trials.
  3. Learn about recent security and bio-security issues arising from new US and EU guidance on improper foreign influence and national security threats.
Knowledge Level: All Levels

Registration
(Deadline May 1)
Late Registration***
(After May 1)

Individual Registration
Member Rate* $99 $114
Non-Member Rate $165 $180
Group Registration**
Member/Non-Member Rate $350 $365

Register for the entire Webinar Series for one low rate!

Registration includes access to the live event, PowerPoint slides, and complimentary access to the On-Demand version for 30-days.
*To receive the member registration rate, you must an SRAI member during the event.
**All Group Attendees must be added when registering. Up to 12 attendees per group.
***If registering late, please contact registration@srainternational.org for assistance.

Online Registration
(Credit Card Payments Only)
  • Click the blue Register button to register for the Webinar
  • Login with your member account or sign up as a first-time visitor
  • Follow the registration instructions and proceed to check out
Full payment must be received prior to the start date of the event. If you have any questions regarding your registration, please contact registration@srainternational.org.

Policies:
Written requests for registration refunds must be postmarked on or before April 25. Cancellations submitted on or before April 25, less a $25 meeting cancellation fee. If you paid membership dues while registering, these will not be refunded; only the actual registration fees will be refunded less the cancellation fee(s). No refunds will be made after April 25. Refunds are not given for no-shows. Registration substitutions from the same institution are accepted; membership substitutions are NOT accepted. All fees will be reimbursed if the program is cancelled. In the case of a cancellation, you will be notified by SRAI from srameetings@srainternational.org.

Registration: We cannot process any advance registration forms without full payment. Invoices will NOT be issued. Purchase orders are NOT accepted. You must be a Full Member of SRA International at the time of the program to receive member rates.

Consent to Use Photographic Images: Registration and attendance at, or participation in, SRA International meetings and other activities constitutes an agreement by the registrant to the use and distribution of the registrant or attendees' image or voice in photographs, videotape, electronic reproduction and audiotapes of such events and activities by SRA International and other third parties.

Privacy Policy: SRA International privacy policy can be found at www.srainternational.org/privacy. For questions email us at communications@srainternational.org.

Contributors

  • Debra Parrish, Partner, Parrish Law Offices, LLC

    Ms. Parrish is an attorney who works with academic medical centers, research institutions and companies, particularly those in the life sciences area in the United States. Her areas of legal concentration are science law (including research misconduct, regulations, compliance and investigations), health care law, and intellectual property. Ms. Parrish previously worked at the Office of Research Integrity as an attorney and now counsels journals, institutions and scientists on matters of research integrity. She is a frequent speaker and author on research integrity issues and has worked on some of the most high profile and complex cases over the past 25 years. In March 2016 she served as an invited panel member on research integrity issues at the National Academy of Sciences. She received her law degree and bachelor of science in biomedical engineering from Duke University and is a member of the patent bar.

May 2, 2024
Thu 2:00 PM EDT

Duration 1H 0M

This live web event has ended.

Support Contact
1 (703) 741-0140 ext. 218