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SUMMARY:2025 BioNTX Legal Forum - Breakfast Briefing
DESCRIPTION:Join BioNTX for breakfast and an engaging Continuing Legal Education (CLE) hosted by Sheppard Mullin at their Dallas office. Explore Prescription Drug User Fee Act (PDUFA) basics\, small business exemptions\, predictions for PDUFA VIII negotiations\, and practical strategies for successful participation. Expand your knowledge and connect with peers in our industry.\nThank you for your support\nSpeakerScott Liebman\, JDCo-Chair\, Life Sciences Practice Chair\, FDA Practice Sheppard MullinScott focuses on complex FDA regulatory\, compliance and legal matters affecting global pharmaceutical\, biotechnology and medical device manufacturers. He counsels clients on federal and state requirements and develops legal and regulatory strategies to help commercialize their products. Clients regularly turn to Scott and his team to support product launches\; implement corporate integrity agreements\; develop comprehensive training and monitor compliance programs\; and handle anti-kickback\, sampling and off-label investigations. Whether advising executives or training a national sales force\, Scott knows that clear\, thoughtful communication and practical advice are key to supporting his clients. He has worked with businesses of all sizes\, from small life sciences organizations launching their first product to Fortune 500 companies in the pharmaceutical and medical products/equipment industries. His clients operate worldwide and include Europe- and Asia-based life sciences companies. Scott is passionate about understanding his clients' challenges and is committed to learning their businesses inside and out to find solutions. He brings deep technical knowledge along with enthusiasm for his clients' work to each client relationship.
X-ALT-DESC;FMTTYPE=text/html:Join BioNTX for breakfast and an engaging Continuing Legal Education (CLE) hosted by Sheppard Mullin at their Dallas office. Explore Prescription Drug User Fee Act (PDUFA) basics\, small business exemptions\, predictions for PDUFA VIII negotiations\, and practical strategies for successful participation. Expand your knowledge and connect with peers in our industry.
Thank you for your support
Speaker
Scott Liebman\, JD
Co-Chair\, Life Sciences Practice Chair\, FDA Practice \;
Sheppard Mullin
Scott focuses on complex FDA regulatory\, compliance and legal matters affecting global pharmaceutical\, biotechnology and medical device manufacturers. He counsels clients on federal and state requirements and develops legal and regulatory strategies to help commercialize their products. \;
Clients regularly turn to Scott and his team to support product launches\; implement corporate integrity agreements\; develop comprehensive training and monitor compliance programs\; and handle anti-kickback\, sampling and off-label investigations. Whether advising executives or training a national sales force\, Scott knows that clear\, thoughtful communication and practical advice are key to supporting his clients. \;
He has worked with businesses of all sizes\, from small life sciences organizations launching their first product to Fortune 500 companies in the pharmaceutical and medical products/equipment industries. His clients operate worldwide and include Europe- and Asia-based life sciences companies. \;
Scott is passionate about understanding his clients&rsquo\; challenges and is committed to learning their businesses inside and out to find solutions. He brings deep technical knowledge along with enthusiasm for his clients&rsquo\; work to each client relationship.
LOCATION:2200 Ross Avenue 20th Floor Dallas TX 75201
UID:e.3812.1104463
SEQUENCE:3
DTSTAMP:20260419T183020Z
URL:https://biontx.growthzoneapp.com/biontx-event-calendar/Details/2025-biontx-legal-forum-breakfast-briefing-1278255?sourceTypeId=Hub
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