UnCharted Access

UnCharted Access

Research Services

New Castle , Deleware 361 followers

Advocacy for All

About us

Welcome to Uncharted Access, where we challenge the often-revisited path to engagement and break through barriers to foster inclusive and impactful change. We believe that inclusion starts at the very core of discovery and extends far beyond the delivery of healthcare. With our unwavering commitment to transforming clinical trials, we are revolutionizing health outcomes for all.

Website
unchartedaccess.com
Industry
Research Services
Company size
2-10 employees
Headquarters
New Castle , Deleware
Type
Self-Owned

Locations

  • Primary

    128 Sunset Blvd

    Suite 1099

    New Castle , Deleware 19720, US

    Get directions

Updates

  • View organization page for UnCharted Access, graphic

    361 followers

     Navigate the complexities of clinical trial planning and conduct with confidence. Unveiling Uncharted Access! We're here to bridge the gap between sponsors and clinical research sites. Our comprehensive site support services ensure smooth feasibility assessments, efficient work-up processes, and expert training programs. Stay tuned for valuable insights and resources to optimize your clinical trials. #clinicaltrials #sitesupport #clinicalresearch

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    What is Hemochromatosis? Hemochromatosis is a genetic disorder that causes your body to absorb too much iron from food. This excess iron can damage organs like your liver, heart, and pancreas. Why Does it Matter for Minorities? Misdiagnosis: Symptoms of hemochromatosis can mimic other conditions, leading to delays in diagnosis, especially for minorities. Lack of Awareness: Lower awareness within these communities can prevent people from getting screened. Genetic Predisposition: Certain ethnicities have a higher risk of hemochromatosis, making early detection crucial. Let's Talk About Hemochromatosis! Educate yourself and your loved ones about the signs and symptoms. Encourage open conversations about mental and physical health within your community. Advocate for culturally competent healthcare that considers your background. Early detection and treatment can make a big difference. Join the conversation and share this post to raise awareness. #MinorityHealth #GeneticDisorders #hemochromatosis #clinicalresearch #clinicaltrials #clinicalresearchjobs

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    361 followers

    Did you know? Minority communities often face unique challenges when it comes to mental health. Cultural stigma, lack of access to care, and underrepresentation in clinical research contribute to these disparities. At Uncharted Access, we are committed to ensuring that mental health treatments are effective for everyone, regardless of background. Diverse participation in clinical trials is crucial to developing inclusive and comprehensive mental health care. Join us this month in raising awareness about minority mental health and the importance of diversity in clinical research. Let’s work together to break barriers and build a future where mental health care is equitable for all. 🔗 Learn more about our mission and how you can get involved: [bio] #MinorityMentalHealth #HealthEquity #InclusiveResearch #ClinicalTrials #DiversityMatters #unchartedaccess

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    361 followers

    Did you know? Hemochromatosis, a condition causing the body to absorb too much iron from the diet, affects 1 in 200 people. Left untreated, it can lead to severe health issues like liver disease, heart problems, and diabetes. At Uncharted Access, we believe in the power of inclusive research to ensure treatments work for everyone. Clinical trials need diverse participants to develop effective therapies for all communities. Join us this month in raising awareness about hemochromatosis and the importance of diversity in clinical trials. Let’s make sure every voice is heard in medical research. 🔗 Learn more about our mission and how you can get involved unchartedaccess.com #HemochromatosisAwareness #HealthEquity #InclusiveResearch #ClinicalTrials #DiversityMatters #UnchartedAccess

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    361 followers

    What's the Deal with Cord Blood? Unveiling its Potential with Inclusive Research. It's July, which means it's #CordBloodAwarenessMonth! But have you heard of cord blood banking or donation? Here's the scoop: Cord blood is the leftover blood in the umbilical cord and placenta after childbirth. It's a treasure trove of stem cells, powerful cells that can develop into different types of blood cells. These stem cells hold promise for treating a variety of illnesses like leukemia, sickle cell disease, and even some immune system disorders. What are your options? Cord Blood Banking: You can choose to store your baby's cord blood for potential future use by your child, a sibling, or even a family member. Cord Blood Donation: Donate the cord blood to a public cord blood bank, where it can be used to help someone in need who's a perfect genetic match. Empowering Decisions with Inclusive Research: This month is all about giving expecting parents the information they need to make informed choices about cord blood. But research on stem cell therapies is constantly evolving, and inclusive research is key to unlocking its full potential. Why Inclusive Research Matters? By including diverse populations in research studies, scientists can develop therapies that work effectively for a wider range of patients. This ensures everyone has a chance to benefit from these lifesaving advancements. #StemCells #Pregnancy #BabyHealth #inclusiveresearch #clinicalresearch #clinicaltrials #clinicalresearchjobs #clinicalresearchcordinator

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    Did you know that June 29th was Rare Chromosome Disorder Awareness Day? Chromosome and gene disorders affect many people, but they're often rare, so many haven't heard of them. This day is about raising awareness and celebrating the amazing individuals living with these conditions. Here are some facts: Chromosome disorders occur when there's an abnormality in the number or structure of chromosomes. Gene disorders happen due to mutations in a single gene. There are hundreds of different types, each with varying effects. Let's be more inclusive. Educate yourself: Learn more about chromosome and gene disorders from trusted sources. Spread awareness: Share this post and use the hashtag #RareChromoDay to help others learn. Celebrate differences: Everyone is unique, and that's something to embrace. Together, we can create a more inclusive world where everyone feels supported. #RareDiseases #Genetics #Diversity #clinicaltrials #clincialresearch #clinicalresearch #clinicalresearchjobs #clinicalresearchsites

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    June is Myasthenia Gravis Awareness Month. While MG may dim someone's physical strength, it doesn't dim their spirit. This year, let's shine a light not just on MG, but also on the need for inclusive research! What is MG? A rare neuromuscular disease that weakens muscles, causing problems like drooping eyelids, difficulty swallowing, and fatigue. Why Does Awareness & Inclusive Research Matter? Early diagnosis, better treatments, and a cure depend on increased awareness and research that reflects the diversity of the MG community. Shine a Light on MG: Here's How! Learn more: Visit the Myasthenia Gravis Foundation Share this post: Help raise awareness about MG and support those living with it. Advocate for Inclusive Research: Demand clinical trials that include diverse participants. #MGStrong: Let people with MG know they're not alone. Together, we can brighten the future for those living with MG through awareness and inclusive research. #mgawarenessmonth #clinicalresearch #minorityhealth #clinicalresearchassociate #clinicalresearchjobs

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    Today, on #NationalHIVTestingDay, we celebrate the power of knowing your HIV status. But the fight against HIV doesn't end there! This year, let's focus on inclusive research to ensure everyone has access to effective treatment. Why is Inclusive Research Critical? Current research doesn't always represent the diverse communities most affected by HIV. This can lead to treatment gaps and unequal health outcomes. Inclusive research ensures new treatments work for all populations. How Can You Make a Difference? Get tested for HIV: Knowing your status empowers you to make informed decisions about your health. Support organizations conducting inclusive HIV research. Demand change: Advocate for policies that prioritize diverse clinical trials. Together, let's build a future with equitable access to testing, treatment, and research for everyone. #NHSTD #EndHIVStigma #minorityhealth #clinicaltrials #clinicalresearch #clinicalresearch #laboratory

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    Today, on International Day Against Drug Abuse and Illicit Trafficking, we recommit to building a world free from drugs, ensuring equitable access to treatment for all. Why Does This Matter? Drug abuse and trafficking have devastating consequences for individuals, families, and communities. Additionally, minority groups often face barriers to accessing effective drug abuse treatment. Addiction destroys lives, but treatment offers a path to recovery. Illicit drugs fuel crime and violence, but equitable access to healthcare saves lives. Millions suffer due to drug-related health problems, but inclusive clinical research can lead to better treatment options for all. Together, we can make a difference! Support Prevention: Educate yourself and others about the risks of drug abuse. Advocate for Treatment: Everyone deserves access to resources for recovery. Demand Action: Support policies that promote public health, safety, and inclusive clinical research to develop effective treatment for all. #WorldDrugDay is a call to action! Share this post and join the movement for a healthier, drug-free future with equitable access to treatment. #clinicaltrials #clinicalresearch #clinicaltesearchjobs #clinicalresearchassociate

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