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
Recorded on: May 24, 2022
Description: Quality management experts Teresa Gorecki and Ken Ray discuss measuring, diagnosing and improving quality culture in your organization. They cover:
- Quality culture as a risk reduction and mitigation strategy;
- Identifying weak systems and structures; and
- Understanding individual and group beliefs within an organization.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Teresa Gorecki, Practice Director, Compliance Architects, and Ken Ray, Co-developer and Practice Lead, Quality Pulse
Recorded on: May 17, 2022
Description: Consultant and former CDER official Radhika Rajagopalan discusses the center’s areas of focus for 2022, including:
- Safety surveillance;
- Quality, effectiveness and safety of generic drugs;
- Misuse of opioid drugs; and
- Data standards.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: Radhika Rajagopalan, consultant, EAS Consulting Group
Recorded on: May 17, 2022
Description: Clinical trial data experts Ching Tian and Sherry Volk present three data trends they have seen in developing decentralized trials (DCT). They discuss:
- Increasing data volume and sources;
- Operational data and insights; and
- The need for better data visibility throughout the course of the trial.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Ching Tian, Senior Vice President, Medable; Sherry Volk, Principal Portfolio Lead, eClinical Solutions
Recorded on: May 10, 2022
Description: FDA regulatory expert Kristin Zielinski Duggan digs into the FDA’s guidance around real-world evidence (RWE) and presents key examples of how this evidence has been used for medical device decisions. She discusses:
- The FDA’s framework for the RWE program;
- The FDA’s April 2021 report on examples of RWE used in medical device regulatory decisions; and
- Using RWE for premarket and postmarket obligations.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: Kristin Zielinski Duggan, Partner, Hogan Lovells
Recorded on: April 28, 2022
Description: Regulatory attorneys Kellie Combs and Josh Oyster discuss the FDA and FTC regulatory frameworks for promotional communications and the enforcement landscape. Topics include:
- FDA requirements and guidances;
- Providing risk-benefit information on social media platforms;
- Third-party social media communications; and
- Endorsements and testimonials.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Kellie Combs, Partner, and Josh Oyster, Partner, Ropes & Gray’s Life Sciences Regulatory and Compliance
Recorded on: April 28, 2022
Description: Electronic systems experts Kent Malmros and Carol Benson discuss implementing a technology to create better organizational governance, change management practices and redefine learning. Topics include:
- Training technology categories;
- Document and content management tools; and
- Benefits of managing all training-related process in one place.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Kent Malmros, Senior Director of Vault Training, Veeva Systems; and Carol Benson, Associate Director of Quality eSystems, Iacyte
Recorded on: April 27, 2022
Description: Device compliance expert Kristen Grumet walks through the FDA’s new proposed Quality Management System Regulation, explaining its provisions and impact. She discusses:
- Conceptual differences between the current Quality System Regulation and ISO 13485;
- Changes in definitions of key terms;
- Which quality system requirements will be more explicit when aligned with ISO 13485; and
- The differences between FDA inspections and Notified Body audits.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: Kristen Grumet, Senior Vice President of Regulatory Compliance, Greenleaf Health
Recorded on: April 20, 2022
Description: Three digital transformation experts discuss the long-term strategy and approach to quality that is needed for cell and gene therapy development. Topics include:
- Emerging treatments;
- Traceability;
- Complex value chains; and
- Specialized talent needs and resource shortages.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Vinod Nela and Rameez Abdul Basheer, Deloitte Smart Quality, and Edward L. Armstrong, Senior Director of Quality Assurance, Mustang Bio
Recorded on: March 30, 2022
Description: A panel of quality experts discusses applying industrial transformation methods to quality systems management. Topics include:
- The stages of industrial transformation;
- Digital transformation of biotech companies’ quality systems;
- The quality management maturity curve; and
- Using data and analytics to drive quality system improvement.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Matthew Littlefield, Cofounder and President, LNS Research; Vivek Murugesan, Senior Research Associate, LNS Research; Jason Boyd, Senior Director, Vault LIMS
Recorded on: March 23, 2022
Description: This webinar shows you how to incorporate cybersecurity into your quality system and defend it to interested third parties. It covers:
- How cybersecurity relates to design controls and the quality system more generally;
- Key tips for defending cybersecurity during an FDA inspection or notified body audit;
- How addressing cybersecurity risk relates to product risk management; and
- What regulatory literature currently exists globally and some of the ways they compare to each other.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: Eric Henry, Senior Quality Systems and Compliance Advisor in the FDA and Life Sciences Practice, King & Spalding