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Best Practices for Managing Regulatory Binders Electronically

$79.00 (Non-Member Price)

$0.00 (SCRS members – Included as member benefit, no additional cost)

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Date and Time: March 17, 2020 @ 12:00 PM ET


Contact Hours: One contact hour will be issued.


Presenter

Trisha Locke, CEO at Keystone Research
Bree Burks, VP of Strategy, Site Solutions at Veeva

Description

Investigative sites looking to reduce administrative burden and improve efficiency are replacing paper-based regulatory binders with electronic systems. Join this webinar to learn best practices and common mistakes to avoid when transitioning to eRegulatory. You will gain insights from industry experts and learn from others that have made the transition to ensure success.

Learning Objectives

●     Understand the industry drivers for change and benefits of electronic systems

●     Review tips for choosing the right system and evaluating a vendor

●     Discover best practices and mistakes to avoid when going electronic


Presenters


Trisha Locke, CEO at Keystone Research

Trisha Locke is a clinical research professional with expertise and 20 years of experience in pharmaceutical and device research and global project management. She is the CEO of Keystone Research, which is internationally recognized as a top ophthalmic clinical research site.

Bree Burks, VP of Strategy, Site Solutions at Veeva

Bree Burks has been involved in clinical research from the perspective of a bedside nurse, research coordinator, team manager and a director of a large central clinical trials office within three leading academic medical centers. As the VP of Veeva’s clinical research site solutions, Bree leverages her industry expertise to develop solutions that meet the complex needs of clinical research sites.


Society for Clinical Research Sites, Inc. is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation.


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To obtain your Contact Hours for this webinar:

  1. The webinar must be watched in its entirety.
  2. The post webinar survey immediately following this webinar must be completed in its entirety.
  3. Your contact hour certificate will be sent to you within 30 days of you viewing this webinar.
  4. The contact hour certificate will be sent to the email address provided when you registered.

Planners, presenters, faculty, authors, and content reviewers do not have any relevant financial relationships with any commercial interest.

This webinar does not imply any endorsement of products or services by the Society for Clinical Research Sites or ANCC.

The materials and recording of this webinar will be available for one year as an archive, but will not award any contact hours.


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