Have questions about some achievements C-Path has accomplished? Whether you’re curious about how we collaborate with stakeholders, or how we’re accelerating the development of new treatments, our FAQs section is a valuable resource designed to give you the insights you need. Have a question we haven’t answered yet? Don’t hesitate to reach out—we’re always here to help and provide guidance. You can find more questions and answers on C-Path's website under FAQS: c-path.org/faqs. #C-Path #FAQs #DrugDevelopment
Critical Path Institute (C-Path)
Research Services
Tucson, AZ 8,734 followers
Advancing Drug Development. Improving Lives. Together.
About us
Critical Path Institute (C-Path) is an independent, nonprofit established in 2005 as a public-private partnership, in response to the FDA’s Critical Path Initiative. C-Path’s mission is to lead collaborations that advance better treatments for people worldwide. Globally recognized as a pioneer in accelerating drug development, C-Path has established numerous international consortia, programs and initiatives that currently include more than 1,600 scientists and representatives from government and regulatory agencies, academia, patient organizations, disease foundations and pharmaceutical and biotech companies. With dedicated team members located throughout the world, C-Path’s global headquarters is located in Tucson, Arizona and C-Path’s Europe subsidiary is headquartered in Amsterdam, Netherlands. For more information, visit c-path.org.
- Website
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http://www.c-path.org/
External link for Critical Path Institute (C-Path)
- Industry
- Research Services
- Company size
- 51-200 employees
- Headquarters
- Tucson, AZ
- Type
- Nonprofit
- Founded
- 2005
- Specialties
- creating collaborations with regulators, patient advocacy groups and the regulated pharmaceutical industry, accelerated development of safer, new medical products, faster, safer, and smarter medical product development, and public private partnership
Locations
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1840 E River Rd # 100
Tucson, AZ 85718, US
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Barbara Strozzilaan 201 1083 HN
Amsterdam, NL
Employees at Critical Path Institute (C-Path)
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Deb Discenza (she/her/hers)
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Thomas Morel
Global Patient-Centred Outcomes Research & Policy Lead at UCB
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Huong Huynh
Regulatory professional collaborating to advance regulatory science and drug development tools | Lead people; Manage projects | Mentor to STEM…
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Hannah Blau
Data Scientist ∙ Research Software Engineer ∙ Listener Extraordinaire ∙ She who does not let stuff fall through the cracks
Updates
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Day 2 of #CGIC2024 included an impactful session led by FDA's Michelle Campbell, and C-Path's Director of Advocacy, Thom Hart. The panel discussed: "Living Experiences in Action: Advocacy Update Across Rare Diseases." Key Highlights from this session included: - Advocacy ensures future generations avoid past struggles. - Involvement in advocacy organizations enhances patient representation. - Incorporating those with lived experience in trial design is essential. - Collaboration among stakeholders can improve patient outcomes. Watch the recording now: https://lnkd.in/gqkkFEvm #CPath #Advocacy #DrugDevelopment #RareDisease
CGIC2024 Day 2 Session: Living Experiences in Action — Advocacy Update Across Rare Diseases
https://www.youtube.com/
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Interested in C-Path updates? Be sure to subscribe at https://lnkd.in/gCNMgWsM For 20 years, C-Path has been providing vital infrastructure to generate a neutral environment for everyone working in drug development to collaborate, not compete. Let's improve lives, together. #CPath #drugdevelopment #neutral #datasharing #globalhealth #collaboration #regulatoryscience
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Dive into this session led by C-Path experts, Joe Hedrick, Executive Director of the Type 1 Diabetes Consortium and Sakshi Sardar, Senior Director of Digital and Precision Medicine as they explore "Transformative Tools to Capture Early Stages of Disease: Digital Health Technologies, Making the Invisible, Visible." Digital health technologies are revolutionizing drug development by unveiling the early, often hidden stages of diseases. These tools are pivotal in enhancing patient outcomes, streamlining drug development, and advancing healthcare delivery. Discover how DHTs are reshaping the future of medicine. Catch the full session here: https://lnkd.in/g6y7x5CA #CPath #InnovationInMedicine #DigitalHealth #DrugDevelopment #HealthcareTransformation #Type1Diabetes #CGIC2024
CGIC2024 Day 1: Transformative Tools to Capture Early Stages of Disease: DHTs
https://www.youtube.com/
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Did you know that you can now donate to C-Path using the Combined Federal Campaign? Are you a Federal employee or retiree? Then GIVE HAPPY to us through CFC using charity code #28364. One of the great benefits of the CFC is that you can give though payroll deduction or through your retiree annuity, giving a little each pay period and supporting our mission all year long. #CPath #CFC #Donate #DrugDevelopment
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Have questions about some achievements C-Path has accomplished? Whether you’re curious about how we collaborate with stakeholders, or how we’re accelerating the development of new treatments, our FAQs section is a valuable resource designed to give you the insights you need. Have a question we haven’t answered yet? Don’t hesitate to reach out—we’re always here to help and provide guidance. You can find more questions and answers on C-Path's website under FAQS: c-path.org/faqs. #C-Path #FAQs #DrugDevelopment
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Have questions about some achievements C-Path has accomplished? Whether you’re curious about how we collaborate with stakeholders, or how we’re accelerating the development of new treatments, our FAQs section is a valuable resource designed to give you the insights you need. Have a question we haven’t answered yet? Don’t hesitate to reach out—we’re always here to help and provide guidance. You can find more questions and answers on C-Path's website under FAQS: c-path.org/faqs. #C-Path #FAQs #DrugDevelopment
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#CGIC2O24 Day 2, Session 2 was moderated by C-Path's Vice President of Rare and Orphan Disease programs, Collin Hovinga. The panel discussed: "A Potential New Framework to Accelerate Drug Development for Rare Diseases." The session emphasized the importance of data sharing in rare disease research, highlighting key initiatives and collaboration for drug development. Watch now: https://lnkd.in/gWfCksSu #CPath #RareDisease #DataSharing #DrugDevelopment
CGIC2024 Day 2: A Potential New Framework to Advancing Drug Development
https://www.youtube.com/
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Interested in C-Path updates? Be sure to subscribe at https://lnkd.in/gjME3Xn6 For 20 years, C-Path has been providing vital infrastructure to generate a neutral environment for everyone working in drug development to collaborate, not compete. Let's improve lives, together. #CPath #drugdevelopment #neutral #datasharing #globalhealth #collaboration #regulatoryscience
Subscribe to C-Path News
https://c-path.org
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C-Path's Cheryl Coon, Vice President of the COA Program, leads a pivotal session on "Navigating Patient-Focused Drug Development (PFDD) Roadmap: Update on the Rare Disease Clinical Outcome Assessment (RD-COA) Resource." The PFDD Roadmap, developed by the FDA, is a groundbreaking strategic framework that amplifies the voices and experiences of patients throughout the drug development process. It’s designed to ensure that new therapies are both scientifically robust and truly patient-centered, aligning treatments with the needs and priorities of those they aim to help. 👉 Watch now: https://lnkd.in/gkv678Y3 #CPath #PFDD #DrugDevelopment #PatientCentered #RareDiseases #HealthcareInnovation #PatientAdvocacy #ClinicalOutcomes #FDA #HealthcareLeadership
CGIC2024 Day 1: Navigating the PFDD Roadmap: Update on the RD-COA Resource
https://www.youtube.com/