Recruitment is essential for generating data on drug efficacy, which is crucial for the approval of new medical treatments. Clinical trial success hinges on the ability to recruit a sufficient and appropriate number of participants.

PicnicHealth is simplifying observational research by combining a direct-to-patient approach, industry-leading AI and technology, and world-class clinical expertise to capture the patient experience in an unprecedented level of detail.

As stakeholders increasingly seek more robust evidence from registries and observational studies, researchers must adopt innovative methods for generating data. Previously restricted by outdated study models, evidence generation can now be more efficient and flexible through the use of cutting-edge technologies, including artificial intelligence. New technology-driven methods frees life science companies from historical constraints, enabling a deeper understanding of the course of disease, drug effectiveness, safety, and quality of life (QoL).

As the life sciences landscape continues to evolve rapidly, the ability to conduct highly efficient yet deeply insightful and reliable research is crucial. PicnicHealth Pulse is specifically designed to address the shortcomings of traditional observational study approaches

PicnicHealth launched its life science product today to enable high-quality, low-burden research for life sciences companies and patients.

Check out this transcript of PicnicHealth’s Chief Scientific Advisor, Dr. Nancy Dreyer, talking with AJMC about how the direct-to-patient approach is superior to traditional observational research methods. She focuses on the collection of better real-world data and how patients can benefit.

PicnicHealth today announced it was ranked among the World’s Best Digital Health Companies by Newsweek and named the “Best MedTech Startup” by MedTech Breakthrough.

Read about how AI is empowering real-world evidence generation in observational research as well as the limitations of using AI within this setting.

Discover what's new at PicnicHealth! Unlock rewards, streamline care team management, track conditions with ease, and explore our latest Pins feature.

Q&A with PicnicHealth Chief Commercial Officer, Rachael Thomas Higgins

Walking through life with salt-wasting congenital adrenal hyperplasia (CAH) brings its own set of ups and downs. For Taylor and her son, Maddox, it’s a path marked by sudden storms and sunny days, a mix of medical emergencies and moments of pure childhood joy. Here’s their story, told with the warmth and honesty that Taylor brings to every conversation.

In this article with PharmaPhorum, our Chief Scientific Advisor, Dr. Nancy Dreyer, provides actionable guidelines on how to integrate direct-to-patient approaches at every stage of your study. See why she believes patient-centric observational research is better fit to answer complex research questions.

PicnicHealth announces the appointment of Rachael Thomas Higgins as Chief Commercial Officer

In honor of Rare Disease Day, we dived into an insightful Q&A session with PicnicHealth's Chief Medical Officer, Daniel R. Drozd, an MD at the forefront of pioneering healthcare research.

As we celebrate Black History Month, we recognize that Black history and the wellness of Black communities must be top of mind every day of the year. Despite the many contributions Black people have made to medicine and wellness, alarming health disparities due to structural and interpersonal racism, still exist for Black people.

PicnicHealth announced the launch of a new study portal to facilitate faster, more accurate observational research.

In celebration of Rare Disease Month, we are thrilled to shine a spotlight on Change Champions, dedicated partners, and organizations making a lasting impact on rare disease research throughout the year. At the forefront of this movement is Rare Patient Voice, a remarkable resource founded with a singular mission – to provide patients and family caregivers a platform to be heard by actively participating in diverse research endeavors, including rare diseases.

In honor of Rare Disease Awareness Month, we're thrilled to kick off our #ShareYourRare campaign. We believe that your stories matter, and through #ShareYourRare, we want to highlight the often-overlooked challenges and stories of those who are living with a rare condition.

Navigating the complex medical landscape is an imposing journey, and it becomes even more challenging when your child is diagnosed with a rare condition like Achondroplasia.

In the heart of Urbana, Ohio, Lydia and her husband Charlie embarked on an unexpected journey that began with the arrival of their daughter, Dagny. Diagnosed with achondroplasia, their story is one of discovery, resilience, and unwavering love.

In a world where each child's journey is unique, Brynn’s story stands out for its strength and resilience. Diagnosed with achondroplasia, Brynn, and her family, have navigated a path filled with challenges, discoveries, and immense love.

The journey of Janet's family into the world of achondroplasia began unexpectedly when their baby girl was diagnosed at four months old.

We’re thrilled to share that #PicnicHealthGivesBack, our annual giving campaign, has returned this year. From now until January 5, 2024, we’re donating to The American Kidney Fund (AKF) and The Chandler Project for each new PicnicHealth sign-up, up to $6k. Join PicnicHealth today to make an even bigger impact.

Life with IgA Nephropathy: What to expect after diagnosis

We partnered with The Chandler Project for an empowering achondroplasia community webinar on how to advocate for your child in a medical setting!