- Sustainability
- DE&I
- Pandemic
- Finance
- Legal
- Technology
- Regulatory
- Global
- Pricing
- Strategy
- R&D/Clinical Trials
- Opinion
- Executive Roundtable
- Sales & Marketing
- Executive Profiles
- Leadership
- Market Access
- Patient Engagement
- Supply Chain
- Industry Trends
US Rep. Introduces Product Information Modernization Bill
August 26, 2015.
U.S. Representative Billy Long (R-MO, 7th District) has introduced a bill to update regulations on how drug manufacturers communicate product information. Long is the lead sponsor of H.R. 2479, which would force FDA to change regulations on how pharma companies share product information with the public. The bill would direct FDA to "clearly regulate meaningful, truthful and non-misleading communication of product information on social media". "One would think something as important as personal decision-making for healthcare would be easy to get economic and scientific data to back up the drug's effectiveness," said Long. "This bill would simply push FDA to update its regulatory approach to communications to keep up with today's technology."
Can Data and AI Deliver Whole-Person Health?
July 9th 2024Executives in the life sciences and medical device industries see promise in artificial intelligence (AI) and medical technologies, but must also navigate the changing healthcare ecosystem, varied stakeholder needs, and the impact of AI on market access and commercialization strategies.
