Regulated healthcare companies are under increasing pressure to move faster while maintaining the highest standards of ...

Creating medical technology products brings with it high risks and cost but can also generate huge rewards. Medical product development combines the challenges of creating systems with ...

Artificial intelligence or AI isn’t going anywhere, and the FDA is the latest agency to recognize its potential to revolutionize healthcare by advancing medical product development, improving patient ...

Paul Levesque, a principal at the management consulting firm MedStar Partners, identifies some key aspects of medical product development. In today's increasingly competitive medical technology market ...

Since its enactment in 2017, Public Law No. 115-92 has significantly boosted the availability of medical products that protect and treat military personnel. Designed to overcome the unique challenges ...

Randomized, controlled clinical trials (RCTs) have traditionally served as the gold standard for evidence generation in support of medical product development and approval. However, it is increasingly ...

The Food and Drug Administration (FDA) defines regulatory science as the science of developing new tools, standards, and approaches to assess the safety, effectiveness, quality, toxicity, public ...

Google’s recent integration of Gemini, its state-of-the-art large language model, into its search engine marks a significant step in AI-driven responses for digital health queries. Worldwide, users ...