Food and Drug Law Institue Inc
Home - Food and Drug Law Institute (FDLI)
131820189
1949
Washington, DC 20005 United States
fdli.org
foodanddruglaw
Food-and-Drug-Law-Institute-333594356849295
702415
Food and Drug Law Institute, Inc.
The Food and Drug Law Institute, Inc. (FDLI) is a nonprofit organization based in the United States, established in 1949. It serves as a prominent membership organization focused on food and drug law, offering a wide range of educational resources, training programs, publications, and professional engagement opportunities for its members. As of now, FDLI's membership encompasses over 30,000 professionals, including manufacturers, distributors, legal practitioners, consultants, academics, government officials, and students across various sectors regulated by the U.S. Food and Drug Administration (FDA) and similar global entities.
Mission and Activities
FDLI functions as a neutral platform for engaging stakeholders in discussions and developments related to public policy, laws, and regulations that affect food and drug law. The organization covers a diverse array of industries that come under FDA's jurisdiction, including:
- Pharmaceuticals
- Medical devices
- Biologics
- Foods and dietary supplements
- Cosmetics
- Veterinary products
- Tobacco and cannabis-derived products
To facilitate knowledge sharing and collaboration, FDLI organizes events such as conferences, webinars, and training courses aimed at enhancing understanding of regulatory frameworks and compliance issues in the sector. These events are designed to foster dialogue among legal and regulatory professionals, thereby influencing policy and regulatory practices.
Education and Resources
FDLI provides a variety of educational opportunities, including:
- Introductory and advanced training courses on FDA laws and regulations.
- Publications that cover recent issues and developments in food and drug law, including scholarly articles and periodicals.
- Webinars that present timely educational content in a flexible format.
These resources aim to enhance the competencies of legal and regulatory professionals and to keep them updated on key developments in the field.
Digital Transformation and Future Directions
In recent years, FDLI has undergone a significant digital transformation, enhancing its technological infrastructure to improve member engagement and operational efficiency. The organization leveraged advanced association management software to automate processes such as event registration and member communications. This transformation has not only streamlined workflows but also increased member satisfaction and participation.
Conclusion
FDLI continues to play a vital role in shaping the landscape of food and drug law through education, stakeholder engagement, and policy advocacy. By providing a forum for discussion and collaboration among various sectors, FDLI helps ensure that legal and regulatory frameworks keep pace with the evolving needs of the industry.
[1] https://www.fdli.org/about/ [2] https://theorg.com/org/food-and-drug-law-institute [3] https://fonteva.com/fonteva-advantage/case-studies/fdli/ [4] https://www.fdli.org [5] https://law.ucla.edu/sites/default/files/PDFs/Publications/_RES_PUB_Food_and_Drug_Policy_Forum_April2015.pdf
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Novinky
Excited to announce a new FDLI webinar happening on May 29! On April 1, FDA eliminated approximately 3,500 positions. What do these reductions and organizational changes mean for how industry engages with FDA on product reviews, postmarket compliance, guidances, and public health research? Panelists will offer insights into FDA’s evolving structure, implications of staff departures on product review and approval, potential disruptions to user fee negotiations, and practical tips for regulated industry on how to move forward during this period of transition. Speakers: E. Cartier Esham, CEO and Founder, Esham Strategies, LLC Danielle C. Humphrey, VP Compliance Officer & Chief Regulatory Counsel, Becton Dickinson (BD) Kurt R. Karst, Director, Hyman, Phelps & McNamara, P.C. Moderated By Rachel Turow, Of Counsel, Skadden, Arps, Slate, Meagher & Flom LLP Register now at http://bit.ly/44AFfmw (fb)
The final countdown is on for the 2025 FDLI Annual Conference! We’re excited to welcome our food and drug law colleagues tomorrow at the Ronald Reagan Building in Washington, D.C. FDLI staff is hard at work putting the final touches in place to ensure a smooth and engaging experience for all attendees. If you haven’t already, be sure to review the agenda and plan your sessions. It’s not too late to join us — in-person or virtually! Register now at fdli.org/annual25. #FDLIAnnual25 (fb)
Poslední komentáře
Absolutely love the initiatives you're taking to educate and empower organizations in the food and drug law field! Knowledge is key to progress! 🍏📚 #FDLIdetail |
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Excited for the upcoming courses! This is such an important step toward ensuring that innovative health products are safe and accessible for everyone. Keep up the great work! 🙌💡 #AdvancingHealthRegulationdetail |
Poslední diskuze
1. How can emerging technologies like AI and machine learning be effectively regulated within the current FDA framework to enhance patient safety and access to innovative healthcare solutions?Odpovědí: 3, Naposledy před 1 den detail |
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2. What strategies can patient organizations employ to better engage with the FDA and influence regulatory decisions that impact their communities?Odpovědí: 3, Naposledy před 1 den detail |
V okolí
25
954
4.5
Washington
O společnosti
- I80 -
News Members Get Involved Upcoming Events Fundamentals of Digital Health Regulation Successfully Navigating Your Product Through FDA Digital health including software mobile health applications machine learning and artificial intelligence AI wearables and personalized medicine has created opportunities to improve patient health and provider efficiency. This course will explore the essentials of FDA regulation of innovative medical device technologies. In this course youll learn whether and how these categories of products are regulated as medical devices. Then the course will cover the various regulatory pathway options for getting a technologically focused product on the market current FDA premarket review initiatives AImachine learning regulations and cybersecurity considerations.
Právní služby
