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ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies. With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!
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Tap into this week's #ProPharmaPolls. #PharmaInsights
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Happy Nurses Month! We're shining a spotlight on David Bezick, at ProPharma. We asked him, "What has been the most rewarding aspect of being a nurse, and how has ProPharma supported you in achieving your professional goals?" Here's what he had to say... #NursesMonth #HealthcareHeroes
ProPharma's Senior Vice President of European Regulatory Development, Lucy Radley (Williams), was recently interviewed in International Clinical Trials (May 2024, pages 38-42), discussing effective partnerships between SMEs and CROs. In her conversation with Samedan Ltd, Lucy addresses common challenges and provides valuable advice on overcoming them. Be sure to check it out: https://lnkd.in/eJ3g7rzZ! #ClinicalTrials #RegulatoryDevelopment #WeAreProPharma
We're thrilled to see Kirk Wroblewski, ProPharma's new #CIO, featured in CIO Online's article. Kirk is an excellent addition to our team, with over 20 years of experience in healthcare data and analytics. We can't wait to see the innovative insights he'll bring to our organization. Read more about his new role and why we're excited to welcome him: https://lnkd.in/eJj_Bmm5. #WeAreProPharma
Maximizing Patient Outcomes: The Ultimate Contact Center Guide With our comprehensive guide, discover the key to building effective patient support programs. Learn how a patient-centered approach and our detailed contact center checklist can transform medication management and elevate patient health outcomes. Download our guide and take the first step toward transformative patient support: https://lnkd.in/e62vrFUk.
Join us at Future Labs Live in Basel next month, where Eliot Randle, Ryan Craig, Alex Butcher, and Kelly Maddison will help you explore ProPharma’s innovative R&D technology. Swing by #ProPharma’s booth #104 on June 26 & 27th—we can't wait to meet you and help you shape the future! #FutureLabsLive
Join myself, Eliot Randle, Ryan Craig, and Kelly Maddison at Future Labs Live in Basel next month, and explore how we can help shape the future of your R&D Technology landscape. We look forward to welcoming you at the ProPharma booth #104 on June 26 & 27th June. Register for tickets >> https://lnkd.in/eQBVVefq #futurelabslive #propharma #informatics #digitaltransformation #automation
📣 Meet Beverly Z., Lead Clinical Systems Consultant, ProPharma 🌟 In her role, Beverly expertly navigates clients through the complex journey of adopting R&D systems. From managing projects to providing support after implementation, she ensures a smooth transition at every stage. Her daily work includes analyzing client requirements, creating user-friendly solutions, and enriching our internal R&D technology knowledge base. Beverly's goal is to align technology with the unique needs of life science organizations. By focusing on compliance and operational efficiency, she empowers clients to push forward in their treatment development, ultimately improving patient outcomes. Read more about Beverly: https://lnkd.in/gG2KpBvE. #MeetTheExpert #WeAreProPharma
You've read Part 1. Now, here's Part 2: Mandatory HTAR Implementation in the EU The Health Technology Assessment Regulation (HTAR) will take effect in January 2025, making mandatory Joint Clinical Assessments (JCAs) and Joint Scientific Consultations (JSCs) for new treatments. ProPharma is your partner for navigating these requirements. Find out how we can guide you through the JCA preparation, submission, and engagement with EU regulatory bodies to ensure your compliance with the new HTAR framework. Read on to learn about the staggered implementation timeline, critical deadlines, and how #ProPharma can support your journey from product development to market launch. Don't miss this in-depth guide to ensure your pharmaceutical company's success under the new HTAR rules: https://lnkd.in/edMeZPCX
Prepare for the New EU Health Technology Assessment Regulation in January 2025! Pharmaceutical companies, get ready for the European Health Technology Assessment Regulation (HTAR), which will take effect in January 2025. This new regulation aims to streamline clinical assessments across the EU and fast-track patient access to innovative treatments. ProPharma can guide you through the #HTAR transition with expert support in regulatory affairs and HTA. Read Part 1: https://lnkd.in/ePFbtXcT, and don't miss Part 2 of our HTAR series for further insights. Stay ahead of the changes and ensure a smooth transition for your products to the European market.
Curious about the latest trends in life sciences? Cast your vote in this week's #ProPharmaPoll on CRS and stay informed! #PharmaInsights
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