Clinical Trials Arena December 19, 2023
Joshua Silverwood

The life sciences sector is set to see a significant amount of change in 2024.

Significant regulatory changes across numerous medical fields are coming in 2024 with pharmaceutical and medical device companies urged to be ready for a year of legal alterations.

From the UK’s reworking of the Voluntary Scheme for Branded Medicines (VPAS) and delayed plans to introduce a new medical device validation scheme, to the United States’ attempt to regulate products that utilise artificial intelligence (AI), 2024 is set to be a busy year for healthcare regulators.

US – Regulating LDTs

Chief among US legal changes set to come into effect in 2024 that has raised concern is the Food and Drug Administration’s (FDA) plan to regulate laboratory-developed...

Today's Sponsors

Venturous
Got healthcare questions? Just ask Transcarent

Today's Sponsor

Venturous

 
Topics: Biotechnology, Govt Agencies, Medical Devices, Pharma / Biotech, Provider, Regulations
The Difference Between a Law and a Regulation in Healthcare, Post-Chevron
Google, Meta execs blast Europe over strict AI regulation as Big Tech ups the ante
The Future of Regulatory Compliance Lies in AI-Powered Tech
AI Regulations: EU Withdraws AI Liability Proposal; US Seeks Comments on AI Action Plan
Europe risks becoming a 'museum' if it doesn't innovate in AI and deregulate, Swedish PM warns

Share This Article