Despite trends and high engagement, pharma companies are still reluctant to invest in disease state educational (DSE) platforms. When will patient preference become the norm? Source: Kantar
关于我们
MPATHIK is a healthcare communications agency that collaborates with patients, medical experts, and advocacy organizations to help our clients introduce therapies that change the world. We listen deeper, we speak truthfully, and we market with heart.
- 网站
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MPATHIK.com
MPATHIK的外部链接
- 所属行业
- 广告服务
- 规模
- 2-10 人
- 类型
- 私人持股
- 创立
- 2024
- 领域
- Healthcare Communications、Engagement Programs、Social + Content、Advocacy Management、Clinical Trial和Story Telling
MPATHIK员工
动态
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Caregivers care ... patiently, endlessly, protectively, with love, and in so many more ways. This November during National Family Caregivers Month, the Caregiver Action Network is encouraging caregivers to share what they're most proud of in their caregiving. Learn more about what's being done this #NFCM and beyond to support the caregivers who give endlessly to others: https://lnkd.in/e2MnMEpg
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Patients are demanding more digital health solutions, and the industry is listening. Investment in digital health offerings has increased over the past two years, resulting in cost-effectiveness and improved outcomes. Source: Peterson Health Technology Institute (PHTI) What digital efforts are you making to keep up with the evolving needs of patients?
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Bringing life-changing therapies to the world requires partnership with those at the heart of the matter. Learn more about how we leverage collaboration to drive greater impact: mpathik.com
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For individuals living with a rare disease, the strength and support of community can be a lifeline. Through Global Genes new RARElyTold Stories toolkit, patients are empowered to share their story through video, driving valuable opportunities for education, emotional support, raising awareness, and more.
Exciting news – we’ve launched our RAREly Told StoriesToolkit, presented by Global Genes and The Disorder Channel! If you’ve wanted to make your own rare disease documentary, this toolkit is the place to start. When your story is out there, people will find it and find you. Some will have faced the same diagnosis. Others may have a different rare diagnosis, but still feel a shared bond. These people might become part of your support network or perhaps collaborators as you work to improve the conditions people face. Whichever way your story goes, access the RAREly Told Stories Toolkit, and learn to share your story on video with the rare disease community! ?? https://lnkd.in/eKJJem3t #CareAboutRare #RareDisease #RareDiseaseAwareness #GlobalGenes #RARElyToldStories #ShareYourStory
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For patients and caregivers, interpreting informed consent forms can be confusing and overwhelming. In an effort to learn from the patient community and ensure clear expectations around trial participation, the FDA is hosting a virtual event on October 30th with the Patient Engagement Advisory Committee. We commend efforts like this, aimed at discussing recommendations on Patient-Centered Informed Consent in Clinical Study of FDA-Regulated Medical Products. Learn more: https://lnkd.in/eErk3Z-H
CDRH Patient Engagement Advisory Committee
fda.gov
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Co-creation allows for strategies rooted in insights, programs that will make an impact, and content that resonates with the community, uniquely solving problems for our clients. Learn more about how we're approaching healthcare communications differently: MPATHIK.com
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For families affected by rare disease, the journey is an endless quest for answers, facing challenges that most are not equipped for. Global Genes is looking to eliminate critical gaps through the launch of their RARE Navigator Pilot Program, which will provide comprehensive case management for each participating family upon diagnosis. ? Learn more: https://lnkd.in/enpbvarW
Global Genes is pleased to announce the launch of our RARE Navigator Program! The six-week program will take a holistic approach to providing support and education to patients by working to understand and address the unique challenges they may face. RARE Navigator will also enable patients and families to effectively share their stories, become confident co-partners in their treatment plans as well as activated advocates within the rare disease community. ?? Learn more by reading the press release here: https://lnkd.in/e5SdVhUv ? #CareAboutRare #RareDisease #RareDiseaseAwareness #GlobalGenes #RareNavigator
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