One of the big questions asked was, "What percentage of your pipeline is externally licensed?" In simpler terms, we wanted to know how much of the new drug developments come from working with other companies. Our panelists shared real-life stories and percentages showing how important these partnerships are. They explained that working together with other companies isn't just talk—it's a crucial way to bring new and better medicines to people. At our recent Global Headquarters launch event in Cambridge, MA, we hosted a fantastic panel discussion on "Transforming Pharma via External Partnerships." #PharmaPartnerships #DrugDiscovery #HealthcareInnovation #Collaboration
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NEW Video 📽: One of the big questions asked was, "What percentage of your pipeline is externally licensed?"In simpler terms, we wanted to know how much of the new drug developments come from working with other companies. Our panelists shared real-life stories and percentages showing how important these partnerships are. They explained that working together with other companies isn't just talk—it's a crucial way to bring new and better medicines to people.At our recent Global Headquarters launch event in Cambridge, MA, we hosted a fantastic panel discussion on "Transforming Pharma via External Partnerships." #PharmaPartnerships #DrugDiscovery #HealthcareInnovation #Collaboration
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Today is #PatientEngagementDay, when we celebrate the crucial role patients play in the biopharma journey. Involving patients early in the process not only fosters trust and collaboration but also drives increased investment and accelerates drug approvals. #PatientEngagement #Biopharma #HealthcareInnovation #PatientCentricity
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Are you moving from phase II to later phase drug developement? If so, are you proactively engaging regulatory operations in your strategy? Connect with IQVIAs regulatory leads today to understand how we can support your strategy. #IQVIA #regulatorycompliance #labeling
Did you know that a proactive approach to artwork creation in preclinical stages helps avoid common mistakes, maximize drug potential, and bring treatments to market faster? From competitor label analysis and aspirational label claims to TPP guidance and early regulatory engagement, IQVIA’s Rama Mohan Rao Chikkam discusses how drug developers can make more informed labelling decisions. Read his insights in full. https://bit.ly/3XvyLBy #drugdevelopment #labeling
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Did you know that a proactive approach to artwork creation in preclinical stages helps avoid common mistakes, maximize drug potential, and bring treatments to market faster? From competitor label analysis and aspirational label claims to TPP guidance and early regulatory engagement, IQVIA’s Rama Mohan Rao Chikkam discusses how drug developers can make more informed labelling decisions. Read his insights in full: https://bit.ly/3Xaupj6 #drugdevelopment #labeling
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Did you know that a proactive approach to artwork creation in preclinical stages helps avoid common mistakes, maximize drug potential, and bring treatments to market faster? From competitor label analysis and aspirational label claims to TPP guidance and early regulatory engagement, IQVIA’s Rama Mohan Rao Chikkam discusses how drug developers can make more informed labelling decisions. Read his insights in full. https://bit.ly/3ZbCXpz #drugdevelopment #labeling
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Did you know that a proactive approach to artwork creation in preclinical stages helps avoid common mistakes, maximize drug potential, and bring treatments to market faster? From competitor label analysis and aspirational label claims to TPP guidance and early regulatory engagement, IQVIA’s Rama Mohan Rao Chikkam discusses how drug developers can make more informed labelling decisions. Read his insights in full. https://bit.ly/3XvyLBy #drugdevelopment #labeling
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Does working with your clinical partners sometimes feel like a massive slog? Do you ever think "why does it always have to be so hard"? What if I told you it doesn't? Join piet theisohn, VP, Clinical Development & Operations Bayer at the inaugural Clinical Partnerships and Outsourcing event this October in London as he shares "Bayer’s Optimized and Cost-Effective Outsourcing Strategy for Clinical Trials" to: - Understand the importance of working together with CROs for Pharma and Biotech, but also the frequent mutual frustration and surprises that come with it. - Explore Bayer's established collaboration model and discover several best practice approaches that you can apply to support on-time, cost efficient clinical trials of high quality. 📅 Download the agenda to find out more: https://bit.ly/4cRXMf3 👉 Book now: https://bit.ly/3XKH90u #ClinicalPartnerships #ClinicalOutsourcing #ClinicalTrials #ClinicalCollaboration #CROs #ClinicalSponsors #Pharma #Biotech
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Did you know that a proactive approach to artwork creation in preclinical stages helps avoid common mistakes, maximize drug potential, and bring treatments to market faster? From competitor label analysis and aspirational label claims to TPP guidance and early regulatory engagement, IQVIA’s Rama Mohan Rao Chikkam discusses how drug developers can make more informed labelling decisions. Read his insights in full. https://bit.ly/4dYu20N #drugdevelopment #labeling
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https://lnkd.in/dM29mT7n 🖇 we bring a wealth of experience in early-phase research and a deep understanding of drug development, from initial stages through post-authorization. 🖇Our team offers strategic guidance tailored to the unique demands of each phase, ensuring you know what is required, when it’s needed, and how to achieve your objectives efficiently. 🖇The dynamic nature of Early Phase Drug Development demands creative and adaptive solutions. We excel at providing these solutions, adapting to the evolving needs of your program with agility and precision. 🖇Our expertise allows us to identify opportunities and overcome challenges, ensuring your pipeline development progresses smoothly. 🖇We pride ourselves on our ability to think critically and act decisively, offering a highly experienced skill set that supports your development goals. 🖇 As your trusted partner, we are committed to bringing innovative strategies and a collaborative approach to drive your success in the competitive landscape of drug development. #DrugDevelopment #PharmaceuticalResearch #EarlyPhaseResearch #ClinicalTrials #BiotechInnovation #PipelineDevelopment #AdaptiveSolutions #InnovativeHealthcare #CriticalThinking
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Patient engagement isn’t optional—it’s essential. Your trials are at risk if you’re not incorporating patient voices into your drug development. 🔍 Patient-Focused Drug Development (PFDD) isn’t a regulatory box to check. As true experts on their conditions, patients provide insights that can make or break your trials. 💡 Why it matters: ✅Higher Success Rates: Patient-centric trials have an 87% launch rate, compared to just 68% for standard approaches. ✅Boosted Enrollment: Understanding and addressing patient needs leads to higher enrollment and retention. ✅Better Decision-Making: Aligning with patient input reduces the risk of late-stage failures and improves regulatory success. 💥 Bottom Line: Trials that ignore patient engagement are likely to fail. Make the patient’s voice central to your strategy—your trial’s success depends on it. #Clinicaltrials #ClinicalTrialEnrollment #DiversityInTrials #Pharma #Biotech --- 🔥I help organizations speed up diverse enrollment by bridging gaps between communities and crucial research. Let's connect!
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Director of Sales, North Star Scientific A life science sales agency helping brands accelerate growth within the biotech, pharma and CRO space. Quality lead generation is what sets us apart.
4moInnovation blossoms through collaboration.