Call for Contributors for Regulatory Documentation Course

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Signup Deadline: 10-Aug-2021
Starts: 16-Aug-2021
Ends: 07-Oct-2021
Location: Online Opportunity


RAPS Online University provides regulatory professionals with education options to hone their skills in specific areas of expertise. We provide individual courses on a variety of regulatory topics, from the basics to product- and region-specific subjects.

We are currently recruiting volunteer experts to participate in the development of a course on regulatory documentation. This course will cover regulatory documentation for various disciplines as described by domestic and international health authorities, along with the roles and approaches to documentation.

The course will also identify various models for collaboration. We hope to incorporate real-life scenarios and stories from seasoned professionals. We are looking for both the medical writer and the regulatory perspective.

RAC holders may claim 3 RAC recertification credits upon completion of this volunteer task. 

This opportunity will close on Tuesday, 10 August 2021. If selected for this opportunity, a representative from the RAPS Online University team will reach out to you directly by mid-August.

To apply for this opportunity:

  • If you're not already logged in, click "Sign in" towards the upper, right corner of this page.
  • Enter your normal log-in credentials or click "Reset your password."
  • Once logged-in, click "Apply Today!" (this will only display after you are logged in).
  • Complete the brief application.


Clinical Trials
Combination Products
FDA meeting and communication strategy
Medical Devices
Preclinical study
Product Lifecycle
Professional Development/Training
Project management
Research, Design and Development

Volunteers Needed:

30 (30 open slots)

Experience Required:

8 - 12 Years Industry Experience

Volunteer Stars:


Recertification Credits:



Wesley Carr
Director of Stakeholder Engagement