This blog explores key considerations for optimizing women’s health research, including improving trial awareness and accessibility, accounting for unique physiological factors, leveraging digital health technologies, and implementing patient-friendly study designs.

The integration of AI into healthcare is and will dramatically change the industry landscape. In order to ensure safety and efficacy in improving health outcomes, we must ensure the SaMDs being developed are both clinically validated and meet notified body requirements.

Learn more about the key takeaways from the FDA's latest draft guidance regarding diversity in clinical trials and what this means for future research.