The Webinar Training Pass

Now get all the training you need – all in one place, and all for one low price!

The FDAnews Webinar Training Pass program gives you year-round unrestricted access to any of the hundreds of webinars listed below. These training programs feature top consultants, expert speakers and FDA officials.

PLUS, subscribers get automatic access to all our new training programs for the next 12 months – that’s more than 50 new programs a year!

If you are already a Training Pass member login below and then scroll down to view the list in date order or narrow your search by keyword or category. Viewing the webinar is easy… simply identify the webinar you want to watch, click on the title and the video will begin. If you would like to view or download the presentation materials separately from the video click the "Download Presentation" link.

Select webinars have been pre-approved by RAPS as eligible for up to 1.5 credits toward a participant’s RAC recertification. Please enter keyword RAPS below for a list of eligible on-demand webinars.

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Webinar Training Pass

Description: Validation expert Rich Yeaton reveals the front-line cleaning validation techniques needed to stay FDA compliant. Yeaton discusses:
  • Developing and implementing a Cleaning Validation Master Plan;
  • The three key parts of a cleaning validation program;
  • Cleaning acceptance criteria; and
  • Appropriate analytical methods.

Presentation: Download presentation

Speaker: Rich Yeaton, President, East Coast Validation Services LLC

Description: Dietary supplements expert Ivan Wasserman discusses how FDA adverse event reporting rules apply to OTCs and supplements just as they do to prescription drugs and explains all facets of the reporting process, including:
  • How to identify adverse events;
  • Collecting data on the event;
  • Documenting the event; and
  • Reporting procedures.

Presentation: Download presentation

Speaker: Ivan Wasserman, Partner, Manatt Phelps & Phillips LLP

Description: Clinical trial specialist Charles Pierce educates research facilities and investigators on how to identify and report on adverse events that occur in their trials and make sure they comply with FDA’s and other authorities’ requirements. Pierce covers:
  • Definitions and types of adverse events;
  • Investigators’ responsibilities;
  • Monitoring and reporting adverse events and managing risk; and
  • Common mistakes in reporting.

Presentation: Download presentation

Handout Adverse Event Study Medication Relationship

Speaker: Charles H. Pierce MD, PhD, FCP, CPI, Pierce One Consulting