?? March is National Blood Disorders Month! Get involved by donating, advocating, or sharing awareness throughout March. #BleedingDisorders #BleedingDisordersAwarenessMonth #RareDisease #MDS #Hemophelia #Leukemia
PatientWing
科技、信息和网络
Philadelphia,PA 2,122 位关注者
Bringing better treatments to more people faster.
关于我们
We are passionate about bringing better treatments to people faster. We work directly with experts in the pharmaceutical industry, helping them enroll rare disease patients every single day.
- 网站
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https://www.patientwing.com
PatientWing的外部链接
- 所属行业
- 科技、信息和网络
- 规模
- 11-50 人
- 总部
- Philadelphia,PA
- 类型
- 私人持股
- 创立
- 2016
- 领域
- Clinical Trials Enrollment和Rare Disease Patient Recruitment
地点
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主要
30 South 17th Street
US,PA,Philadelphia,19103
PatientWing员工
动态
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Many patients first learn about clinical trials online, yet research sites often lack the digital presence needed to reach them. Websites, social media, and patient-friendly content can make all the difference in accelerating enrollment. We’re seeing firsthand how sites that proactively advertise their trials online experience higher engagement and faster enrollment. What’s working for your site? Are there barriers preventing you from going digital? Let’s discuss! ??
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This Women’s History Month, we’re shining a light on some of the remarkable women who have shaped clinical research and healthcare policy. Their contributions have led to groundbreaking treatments, improved patient care, and more inclusive medical advancements. Take a moment to learn about the pioneers who have made a lasting impact in our field—and join us in celebrating their achievements! ??? #WomensHistoryMonth #ClinicalResearch #WomenInScience #HealthcareInnovation #PatientWing
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Curious how we accelerate enrollment for rare disease and serious conditions clinical studies? #PatientEnrollment #ClinicalResearch #PatientWing
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Multiple sclerosis (MS) is a complex and often unpredictable condition, impacting nearly 1 million people in the U.S. alone. PatientWing is committed to supporting MS patients by making research opportunities more accessible and ensuring they have the resources needed to make informed decisions about their health. ?? During MS Awareness Week, take a moment to: ?? Learn more about MS and its impact ?? Support MS-focused research and advocacy efforts ?? Share resources with those affected #MSAwarenessWeek #MultipleSclerosis #ClinicalResearch #PatientAdvocacy #MSCommunity #PatientWing
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Myth: Clinical trials are only for people who have run out of treatment options. Fact: Many clinical trials are designed for newly diagnosed patients, those looking for alternatives, or even healthy volunteers! We know there’s a lot of misinformation about research studies, which is why we’re here to answer your questions and clear up misconceptions. What’s a clinical trial myth you’ve heard before? #ClinicalTrialFacts #MythVsReality
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We’re launching a new blog series! ?? We understand that navigating clinical trials—whether as a patient, caregiver, or sponsor—comes with a lot of questions. That’s why we’re launching a blog series designed to shed light on key topics in patient recruitment, clinical research, and emerging therapeutics for patients. Our first post is already live! ?? We’re diving into Challenges and Opportunities in Multiple Sclerosis Clinical Research: A Path Forward, packed with insights and real-world solutions. Check it out here: https://lnkd.in/evWvDbxX #ClinicalTrials #PatientRecruitment #PatientEngagement #PatientWing
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Rare Disease Day: Every Voice Matters in Clinical Research Rare disease patients face unique challenges, and their participation in clinical trials is often driven by hope—for themselves and for future generations. This Rare Disease Day, let’s shine a light on how sponsors, research sites, and family/friends can make a meaningful difference. ?? Support can be simple yet powerful: ? Sponsors: Design patient-friendly studies with clear communication. ? Research Sites: Create welcoming environments with flexible, compassionate care. ? Family & Friends: Offer emotional support and practical help every step of the way. ?? Check out our infographic to see actionable ways we can all support rare disease patients in their clinical trial journeys. Together, we can make research more inclusive, accessible, and human-centered. #PatientWing #RareDiseaseStudies #FindaCure #PatientEnrollment
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80% of clinical trials struggle with recruitment delays. For biopharmaceutical companies, that means higher costs, longer timelines, and potential setbacks in bringing life-changing therapies to patients. PatientWing works alongside sponsors to tackle these challenges head-on—leveraging grassroots outreach strategies, advocacy group connections, and personalized patient support. What’s your biggest recruitment challenge in 2025? Let’s discuss. ?? #PatientWing #ClinicalTrials #PatientEnrollment #Biopharma #ClinicalOperations
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We’re at the Site Council Leadership Forum and excited for the conversations ahead! We know that clinical research sites are at the heart of patient enrollment, and we’re looking forward to connecting with leaders to share ideas, challenges, and solutions that make recruitment smoother for everyone. If you’re here, let’s chat! ??
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