In consumer health, clinical evidence is now the currency of competitive advantage. Whether you’re defending premium positioning, accelerating time-to-claim, or standing out in crowded categories, generating credible, defensible data fast is key to market success.

This webinar brings together innovative consumer health leaders to explore how modern study designs, from decentralized trials to real-world evidence approaches, are redefining claim substantiation.

Clinical trials for consumer health products encompass a wide range of categories, including dietary supplements, OTC medications, wellness applications, and skincare. These studies cannot follow the same "one size fits all" approach as traditional pharmaceuticals — they require tailored recruitment and patient engagement strategies to generate data for health claims, so consumers can feel secure knowing the products they use are both clinically validated and effective.In this webinar with Habitual, we explore how to design and execute effective studies for consumer health products — with a focus on smart recruitment, patient engagement, and generating the right evidence to support marketing and health claims. Learn what it takes to run fast, flexible, and science-based trials that deliver trust and results.

This webinar explores methods for enhancing clinical trial operations for women’s health indications while putting patients at the center. We delve into critical considerations for reproductive health, participant recruitment, the importance of tailoring trials to meet the unique needs of women, and more. This discussion also features a case study on STAMP, our clinical trial with Daye that is evaluating the performance of a diagnostic tampon in detecting human papillomavirus (HPV) and other sexually transmitted infections (STIs).🍊 Learn more about Lindus Health:https://www.lindushealth.com

💻 Watch the webinar:

https://www.youtube.com/watch?v=nF1g4Ad9X-Y

Join Lindus Health, Glucotrack, and Motif Neurotech for a deep-dive into the most common pitfalls traditional Contract Research Organizations (CROs) make when running medical device trials—and what leading innovators are doing differently. In this session, industry experts unpack why standard approaches often fall short for devices, covering everything from misaligned trial models to logistical and regulatory hurdles.You’ll learn:

• Why traditional CRO models struggle with device trials
• Key operational and regulatory challenges—and how to overcome them
• Actionable strategies for faster, more effective device research

Watch the webinar here: https://www.youtube.com/watch?v=v95ulKYrKi0