Advancing LGBTQIA+ Representation: The FDA’s Role in Inclusive Diversity in Clinical Trials

Advancing LGBTQIA+ Representation: The FDA’s Role in Inclusive Diversity in Clinical Trials

Inclusive clinical trials are essential for ensuring that new treatments and medical interventions benefit all populations, particularly those historically underrepresented in research. By addressing barriers such as non-inclusive screening processes and lack of awareness in LGBTQIA+ communities, the FDA is making strides toward more diverse and representative clinical trial cohorts. This commitment to inclusivity will help create safer, more effective treatments that reflect the needs of all individuals, regardless of gender identity or sexual orientation.

read more
What is a Label Comprehension Study?

What is a Label Comprehension Study?

Label comprehension studies test how well a typical consumer can understand the labeling for an over-the-counter (i.e., non-prescription) drug or medical device. The labeling may include the product box or the instructions for use found inside the package. The idea is...

read more
FDA User Comprehension Studies

FDA User Comprehension Studies

What is an FDA user comprehension study? The US Food & Drug Administration (FDA) is responsible for identifying and mitigating consumer risks associated with the products it’s charged to regulate. This includes both prescription products and those sold...

read more