The FDAnews Webinar Training Pass program offers year-round, unrestricted access to any of the hundreds of webinars listed below. These training programs feature thought leadership and best practices from top consultants, expert speakers and current and former FDA officials. New webinars are offered every month, along with access to the Webinar Training Pass archive.
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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.
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Webinar Training Pass
Description: Attorney Frederick Stearns explains the FDA's new "general wellness" classification for medical devices and apps. He discusses:
- How to make sure your health claims are "wellness" not "treatment" claims that will run afoul of the FDA's rules;
- How to be sure your device satisfies FDA criteria for low-risk treatment; and
- How to apply the agency's five-step test to determine whether your device falls under the FDA's general wellness exemptions.
Presentation: Download the presentation
Speaker: Frederick Stearns, Partner, Keller and Heckman
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: GMP trainer Joanne Cochran offers guidance on training subject matter experts to face subject-specific teams of FDA investigators under the agency's new inspection plan. She covers:
- How to be assured your SMEs are aligned to the topics they are going to be asked about;
- Improving SME effectiveness by conducting thorough simulated inspection scenarios; and
- Examples of questions commonly asked by investigators and answers that are typically found satisfactory.
Presentation: Download the presentation
Speaker: Joanne Cochran, President, JWC Training Associates
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: Attorney Scott Cunningham helps regulatory affairs and clinical trial management teams to prepare for upcoming changes in clinical trial data reporting. Topics include:
- Assuring that entries in ClinicalTrials.gov are consistent with internal records and addressing gaps in reporting;
- Determining when the 21-day rule begins;
- The ramifications of submitting trials on off-label drugs; and
- How much data is expected for adverse events.
Presentation: Download the presentation
Speaker: Scott Cunningham, Partner, Covington and Burling, LLP
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: Regulatory affairs expert Mukesh Kumar teaches how to structure a risk-based raw materials management program suited for the GMP environment. Topics include:
- FDA's expectations regarding raw material vendor selection;
- Proven and cost effective measures for assuring acceptable quality of materials;
- Sampling and assurance documentation quality control units expect; and
- Training requirements for frontline employees and managers.
Presentation: Download the presentation
Speaker: Mukesh Kumar, Regulatory Affairs and Quality Assurance, Amarex
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: Supplier management expert Jeff Kasoff offers proven techniques for complying with FDA QSR and ISO 13485 supplier management requirements. He covers:
- The latest interpretation of QSR and ISO 13485 requirements for supplier selection and assessment — and how US and EU investigators are applying it during inspections;
- How to on-board and qualify new suppliers in a cost-efficient manner; and
- Innovative assessment techniques for current suppliers.
Presentation: Download the presentation
Speaker: Jeff Kasoff, Director of Quality, Medivators
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: Drug and device expert Lynn C. Tyler explains the potential impact of the FDA's final guidance, "Circumstances that Constitute Delaying, Denying, Limiting, or Refusing to Permit Drug Inspection." He provides:
- Legal and operational strategies for responding to FDA's assertion of increased authority; and
- Best practices for coordinating between the investigator, regional office and FDA headquarters if disagreements arise in the conduct of an inspection.
Presentation: Download the presentation
Speaker: Lynn C. Tyler, Partner, Barnes and Thornburg, Food, Drug and Device Law Practice Group
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: Regulatory expert Michael Swit uses FDAnews' exclusive FDA Form 483 database to demonstrate how analyzing these documents can help you prepare for your next inspection. He discusses:
- What can be learned from examining 483s;
- How to respond to a 483; and
- FDA expectations.
Presentation: Download the presentation
Speaker: Michael Swit, Special Counsel, Duane Morris LLP
Description: Consultant John E. Lincoln teaches how to keep your audit program on track and effective. He explains how to:
- Enhance organizational awareness of internal audit requirements;
- Best conduct the audits; and
- Properly document and present the results during inspections.
Presentation: Download the presentation
Speaker: John E. Lincoln, Principal, J.E. Lincoln and Associates, LLC
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: Attorneys Jonathan Kahan, Kristin Zielinski and Kelliann Payne explain in detail the FDA's new one-step de novo reclassification procedure and how to assure that your petition includes all the required data elements and supporting research the FDA has requested. They cover:
- FDA's evolving view of substantial equivalence and de novo reclassification;
- When a de novo reclassification petition is appropriate; and
- When and how to use the pre-submission process.
Presentation: Download the presentation
Speakers: Jonathan Kahan, Partner and Co-director, Food, Drug, Medical Device and Agriculture Group, Hogan Lovells; Kristin Zielinski, Director of Regulatory Sciences, Hogan Lovells; and Kelliann Payne, Counsel, Hogan Lovells.
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant's RAC recertification. Upon full completion please email customerservice@fdanews.com for certificate of attendance.
Description: Award-winning compliance expert John Avellanet presents a 16-step approach for inspection preparation. Topics include:
- How an FDA investigator prepares for an inspection;
- Workflow of the inspection - from the FDA's perspective; and
- Seven steps to immediately take upon receiving FDA notification of an inspection.
Presentation: Download the presentation
Speaker: John Avellanet, Founder, Cerulean Associates, LLC