Cour Pharmaceuticals Development Co., Inc.’s Post

🧠 During #BrainTumourAwarenessMonth we’re taking this opportunity to let patients know how they can discover all possible treatment options with myTomorrows. 💚 Discovering and accessing a clinical trial is just a four-step process with our patient navigators. Know your options here https://lnkd.in/enzyTP4u #BTAM #clinicaltrials #BrainCancer #BrainTumour #BrainAwarenessWeek

We drive advancements in how this disease is cared for. One way we do this is through our our "International Expert Clinical Case series" (IECC). Launched in 2021, our IECC series helps drive discussion and collaboration amongst the #HHT medical community. Hosted by Cure HHT and held bi-monthly, each virtual meeting focuses on a different and specific topic area of HHT -- from brain to lung to spine to liver and more. Challenging cases are presented, and experts from around the world discuss and debate best practices and standards of care -- all in the name of driving better patient outcomes. Learn more about how we drive impact: https://lnkd.in/gDEyhNP9

Knowledge is Power! Patients with MDS can learn from Dr. Hetty Carraway in this recent Seattle Patient and Family Conference recording. Families of these patients can understand more, too, by watching here: https://lnkd.in/eSDTbcYA #MDS #bloodcancer

Blood-based CRC screening is easy and less invasive than other traditional methods. Getting screened is so important and anyone age 45+ should get screened and have a baseline for future screenings. Let's get tested and increase survival rates!

Parexel's Rare Disease Patient Advisory Council met last week ─ just in time for #RareDiseaseDay! The Council explored the role of artificial intelligence in rare disease healthcare and clinical trial research — discussing the benefits, challenges and potential concerns of its use. Huge thanks to our amazing patients and advocates for their ongoing collaboration through our Patient Advisory Councils. Your insights help us shape patient-focused trials that prioritize patient needs. 🤝💡 #RareDiseaseAwareness #AIinHealthcare #PatientAdvocacy

As World Sepsis Day is approaching, we have prepared a dedicated webinar with professors Jean-Louis Vincent and Zsolt Molnar, who will discuss specific treatment options in sepsis. Join us and use the opportunity to address your questions to world renowned experts. See you tomorrow!

Have you ever wondered how you can help advance research without participating in a clinical trial? Patient research registries may be the answer! In this blog, Melissa Calise describes the basics of a patient registry, why they are important to healthcare and how you can get involved with our registry - the HEADS Registry. Read now: https://lnkd.in/ekvvRMCN

Did you know that Rare Patient Voice can recruit rare and non-rare disease patients for clinical trials? Our community is large, always growing, and eager to take part in all kinds of research! #ClinicalResearch #ClinicalTrials #TrialParticipants

Save the date, RSVP, share with your networks to learn more about Nodify Lung and IQLung! #Biodesix #LungCancer #NodifyLung #IQLung

With the recent updated FDA guidance on Clinical Trial Diversity - the one thing that stands out for me is the need for DATA. Data Sources, Data Access, Data Quality. Your Epidemiology plan needs to be Data Driven. You will need to have a robust data source of the highest Quality - the FDA WILL review this. You will need to include an overview of your Patient Engagement and Recruitment Strategy - and this has to involve appropriate site selection with a patient community that supports your desired real-world population. Finally, don't forget, it's not just about Age, Ethnicity, Sex, Race........ When we create offerings @Citeline, we ensure they solve a genuine industry need. #FDA #Diversity #ClinicalTrials #Data #Citeline