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.
BUY NOW Single-User 1-Year Unlimited Access $1,362
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.
Also available: Take advantage of our multi-user and site licenses of the Webinar Training Pass, so you’ll have the most-informed workforce! Contact Russ Titsch, Business Development Director at russ.titsch@wcgclinical.com or +1 703.538.7651 to receive a custom quote.
Search by keyword, speaker name or just by category (drug, device or clinical) and you'll find all you need.
If you have any questions or are having any problems please give us a call on 703.538.7600 or email customer service.
Webinar Training Pass
Recorded on: Sept. 20, 2022
Description: Medidata’s Olgica Klindworth, senior director of R&D, and Anne Rosenberg, director of RBQM solution services, explain how to make the data in your DCTs and modern trials work for you, enabling you to:
- Take control of the increasing volume and velocity of data within today’s clinical trials and use it to your advantage;
- Understand the common myths around data quality oversight in decentralized and hybrid clinical trials so you can increase clinical trial success; and
- Recognize and implement tools for executing effective and efficient clinical monitoring strategies as part of modern clinical trials.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Olgica Klindworth, Senior Director, R&D, Medidata; Anne Rosenberg, Director of RBQM Solution Services, Medidata
Recorded on: Sept. 20, 2022
Description: Today’s design and quality experts take a different approach to designing high quality medical devices. Industry experts discuss:
- Overcoming the costly impact of ineffective requirements management;
- Meeting compliance challenges with closed-loop digital traceability throughout the development and design process;
- Encouraging a proactive and risk-based approach to prevent the occurrence of problems in advance of its manifestation; and
- Using the collected data from a QMS to make proactive and informed decisions.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Sandra K. Rodriguez, Senior Industry Analyst, Axendia; Jeffrey Caltrider, Principal Engineer with R&D New Product Introduction, Enterprise Life Sciences Company; Vinod Nela, Leader Supply Chain & Network Operations, Deloitte Enterprise Performance; Nikki Willett, CSO/VP of Industry Solutions & Digital Transformation, ComplianceQuest
Recorded on: Sept. 15, 2022
Description: With a new commissioner and his staff on board at the FDA, with PDUFA VII about to be implemented, with a new normal developing as the pandemic wanes, there will be significant changes at the FDA that will affect every stakeholder. The speakers share:
- What new provisions in the user fee legislation will affect your daily business;
- Importance of the recent drug importation guidance and the impact of new guidances;
- How key personnel changes at FDA will impact you; and
- Impact of drug-related “crises” on CDER’s approach to R&D and approvals.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Wayne L. Pines, Member of International Advisory Council and President of Healthcare, APCO Worldwide; Deborah Livornese, Director, Hyman, Phelps & McNamara, P.C.; Lowell M. Zeta, Partner in the Life Sciences and Global Regulatory, Hogan Lovells US LLP; Eva Temkin, Partner, King & Spalding FDA and Life Sciences; Kevin M. Madagan, Partner, Reed Smith
Recorded on: Sept. 14, 2022
Description: This webinar dives into the impact data strategy alignment can represent and how digital maturity awareness can help life science companies get a jump start on omnichannel engagement. You’ll learn:
- Why leveraging structured data through omnichannel is a best practice — and how to transform your unstructured data;
- Why breaking down silos and disparate systems can accelerate omnichannel success by increasing internal alignment and awareness to harmonize the digital experience platform (DXP);
- How using AI, ML, and NLP can enhance the RWD insights you need for your brand; and
- How segmentation targeting through synchronized channels with personalized engagement can increase market access, brand loyalty, and drive ROI.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Steve LoSardo, Vice President, Life Science Solutions and Consulting, SoftServe; Georgi Bilyukov, Director, Digital Experience Platforms, Centers of Excellence, SoftServe
Recorded on: Sept. 13, 2022
Description: Trial master file expert Laura Wiggins takes the stress out of your TMF inspection preparedness, explaining how to organize and mobilize your team for a smooth inspection. You’ll learn:
- How to overcome the main challenges of inspection preparedness, including lack of experience with regulatory inspections, lack of understanding regarding records requirements and poor documentation;
- What to do when you’re missing TMF documentation, don’t have a study team or when you’ve had a lack of study oversight; and
- How to use strategic thinking models.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: Laura Wiggins, TMF Services Project Manager, Just in Time GCP
Recorded on: Sept. 8, 2022
Description: Get control of your data by learning the basics of developing best practices and SOPs that turn inspection nightmares into routine management tasks. You’ll cover:
- The legal basis of FDA records access authority, including what FDA can’t access;
- Types of documents commonly requested during inspections;
- Problems and pitfalls to avoid; and
- The Top 10 questions to ask about your archival process.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: David L. Chesney, Principal, General Manager, DL Chesney Consulting, LLC
Recorded on: Aug. 25, 2022
Description: Without proper due diligence, life sciences companies may wind up with a returned product that does not meet the necessary standards for quality. This webinar covers:
- Regulatory requirements for raw material suppliers;
- Definitions of differ types of materials;
- Different risk attributes; and
- How to consider risk attributes to manage suppliers using a risk-based approach.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: Bob Mehta, Principal Consultant, GMP ISO Expert Services
Recorded on: Aug. 10, 2022
Description: This webinar enables you to understand and comply with the FDA’s gene and cell therapy requirements and avoid common errors, so you can maintain your products’ critical quality attributes and bring them to market. You’ll learn:
- FDA requirements for comparability studies for gene and cell therapy products;
- Best practices for risk analysis and mitigation using comparability studies; and
- How to design an effective comparability protocol for a gene or cell therapy product.
Presentation: Download the presentation
Transcript: Download the transcript
Speakers: Scott R. Burger, MD, Principal, Advanced Cell & Gene Therapy; and William E. Janssen, PhD, Principal, WEJ Cell and Gene Therapy Consulting Services
Recorded on: Aug. 9, 2022
Description: Legal and regulatory expert Michael Gaba details the avenues that you can take to achieve a successful premarket review from the FDA, including:
- FDA premarket review pathways;
- Breakthrough device designation and STeP; and
- Medical coverage of innovative technology (MCIT) pathway.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: Michael Gaba, Vice Chair of FDA Practice, Polsinelli
Recorded on: Aug. 3, 2022
Description: John E. Lincoln, principal of J.E. Lincoln and Associates shares how to develop, validate and refine your pharmaceutical process validation processes to ensure their reliability, consistency and efficacy when you:
- Understand the key points in the FDA’s process validation guidance document;
- Appreciate the value to your company when you put these principles into practice; and
- Recognize the key process, equipment (production/test/lab), hardware and software, and QMS/21 CFR 11 verification and validation activities.
Presentation: Download the presentation
Transcript: Download the transcript
Speaker: John E. Lincoln, Principal, J.E. Lincoln and Associates