💊 AI and Computational Models for Drug Discovery and Target Identification Listening to Dr. Giedre Kvedaraviciene at the 1st EP PerMed Implementation of Personalised Medicine School – “Data-Driven Research and Implementation” was both insightful and thought-provoking. She highlighted how AI and computational models are reshaping drug discovery and development, offering real opportunities to accelerate timelines, reduce costs, and enhance target identification—ultimately moving us closer to truly personalised therapies. With almost 30% of the world’s data now generated by the healthcare sector, we are surrounded by an unprecedented wealth of information. Yet, unlocking its value requires not only advanced tools but also a shared vision of responsible innovation. Dr. Kvedaraviciene also reminded us of the regulatory complexities ahead: the overlap between the AI Act and the Medical Device Regulation (MDR), and the differences in risk management, dataset governance, and validation standards across regions. These challenges underscore the importance of collaboration between scientists, regulators, and policymakers to ensure safe and ethical progress. As AI continues to advance, keeping patient benefit and trust at the centre will remain essential. #PersonalisedMedicine #AIinHealthcare #DrugDiscovery #EPPerMed #HealthInnovation
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The AI Drug Trial Revolution: Faster, Safer, Smarter! 💊🤖 Step into the future of medicine with our 2-minute animated short, “The AI Drug Trial Revolution: Faster, Safer, Smarter!” Discover how artificial intelligence is reshaping drug development—making clinical trials more efficient, precise, and patient-friendly than ever before. With vivid Kodachrome-inspired visuals and a young British narrator guiding you through every breakthrough, this film reveals how AI is accelerating discovery, reducing risk, and paving the way for life-saving treatments. Join us on this transformative journey and see how technology is rewriting the story of medical research. If you’re passionate about innovation in healthcare, like and share to spread the vision of a smarter, safer future in medicine! 📩 Let’s connect — reach out to ian@itconsultingroup.com for insights, collaborations, or speaking opportunities. #AIDrugTrial #HealthcareInnovation #AIinMedicine #ClinicalResearch #FutureOfHealthcare #DigitalHealth #MedicalAI
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The AI Drug Trial Revolution: Faster, Safer, Smarter! 💊🤖 Step into the future of medicine with our 2-minute animated short, “The AI Drug Trial Revolution: Faster, Safer, Smarter!” Discover how artificial intelligence is reshaping drug development—making clinical trials more efficient, precise, and patient-friendly than ever before. With vivid Kodachrome-inspired visuals and a young British narrator guiding you through every breakthrough, this film reveals how AI is accelerating discovery, reducing risk, and paving the way for life-saving treatments. Join us on this transformative journey and see how technology is rewriting the story of medical research. If you’re passionate about innovation in healthcare, like and share to spread the vision of a smarter, safer future in medicine! 📩 Let’s connect — reach out to ian@itconsultingroup.com for insights, collaborations, or speaking opportunities. #AIDrugTrial #HealthcareInnovation #AIinMedicine #ClinicalResearch #FutureOfHealthcare #DigitalHealth #MedicalAI
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🌍 AI is Transforming the Future of Drug Development and Clinical Trials 💊🤖 Every day, I feel more inspired by how Artificial Intelligence is reshaping the landscape of clinical research and drug development. From predicting molecular interactions to optimizing trial design — AI isn’t just improving efficiency; it’s redefining how we approach healthcare innovation. ✅ Smarter Discovery: AI models identify promising molecules faster than traditional lab methods. ✅ Better Trials: Intelligent algorithms help select the right patients, predict outcomes, and minimize trial failures. ✅ Safer Care: Real-time analytics enhance patient monitoring and safety across every phase. ✅ Informed Decisions: Data-driven insights are helping scientists, clinicians, and regulators move with greater confidence. The future of drug development is not only faster but also more precise, ethical, and patient-focused. 💭 I truly believe the collaboration between data science and medicine will define the next era of healthcare innovation. #AI #ClinicalResearch #DrugDevelopment #HealthcareInnovation #DigitalHealth #DataScience #Pharma
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Super insightful deep dive into how clinical trials can leverage AI to optimise administrative and manual tasks whilst keeping human in the loop. #AI #MedTech #engineering #research
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Medical Affairs stands at a crucial juncture, with the future of patient care depending on transforming vast data into decisive action. The new BIP’s whitepaper, "Medical Affairs in the Age of Agentic AI," explores how Agentic AI is fundamentally reshaping the function. Discover how these autonomous, adaptive systems are empowering Medical Affairs to: Close treatment gaps and proactively identify unmet patient needs. Revolutionize insight generation, literature summarization, and predictive stakeholder engagement. Tailor actions and content to stakeholder behaviours. Create concise, high-quality summaries at scale Download our whitepaper here: https://ow.ly/jLBP50XakWK #MedicalAffairs #AgenticAI #LifeSciences #HealthcareAI #DigitalHealth #AIInnovation #Whitepaper #Biopharma #Pharma BIP xTech
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Accelerating the use of #technology in #clinicalresearch was a resounding theme at this year’s DPHARM: Disruptive Innovations to Modernize Clinical Trials conference, notes Lyn Agostinelli. How exactly? Read her key takeaways for more on advancing technology and #AI in clinical research, while providing a balanced look at opportunities and precautions, so we don’t lose focus on patients and internal stakeholders. Read more👉https://bit.ly/4nV7xPi #ClinicalDevelopment #ClinicalOperations #DPHARM #ArtificialIntelligence
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AI is changing drug discovery. This white paper shows how integration, not just algorithms, creates real value for drug developers, featuring: · Lab-in-the-loop workflows · Stronger data continuity across R&D · Real-world use cases See where AI drives speed, cost, and precision, and learn what’s next for personalized medicine. Download a free copy. https://okt.to/6smlbQ #AIDrugDiscovery #DrugDiscovery #AIinPharma #PharmaInnovation #LabOfTheFuture #SmallMoleculeDrugDiscovery #MachineLearning
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Great panel at the nference Agentic AI Innovation Summit on The Future of Agentic AI in Biomedical Innovation. I really enjoy participating on panels such as this. The preparation and co-panelists really make me think about the thoughtful questions being ask. Today's conversation about AI autonomy and accountability and scientific and operational oversight built for distributed agency didn't disappoint. The Hard Truth: Accountability Can't Be Diffuse When Consequences Are Real As we deploy agentic AI across drug development, from target identification to trial optimization, we need more than philosophical frameworks. We need infrastructural redesign. I believe in a layered liability model: → Model builders own validity → Deployers own contextual fitness → Sponsors own ultimate clinical and regulatory accountability But here's what makes this real: algorithmic audit trails as rigorous as our data audit trails. Every agent action must be reconstructable detailing what it saw, what logic it applied, and what oversight was present. On Scaling Responsibly: We Need Boring Infrastructure, Not Just Brilliant Algorithms Let's be clear: almost all healthcare interventions are regulated and reviewed by the FDA or some government agency. While not every agentic AI application needs this level of scrutiny, any system making critical patient health decisions absolutely must be. We can't carve out exceptions just because the technology is novel. Three non-negotiables: Validation frameworks matched to risk profile. A model suggesting targets needs different validation than one executing dose calculations. We need FDA-grade pathways tiered by consequence, not novelty. Human checkpoints at irreversible decisions. Agents can propose and execute within bounds, but any action that locks in patient exposure or regulatory commitment needs a human signature. Cultural honesty about optimization goals. Are we saving time? Reducing bias? Cutting costs? Vague claims about "augmentation" erode trust faster than honest trade-offs. Bottom line: We scale when systems are more auditable than the humans they replace and not more opaque. #AgenticAI #BiomedicalInnovation #DrugDevelopment #AIinHealthcare #RegulatoryScience #ResponsibleAI
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Artificial intelligence (AI) has shown enormous potential to transform the drug development process and healthcare practices. Generative AI (GenAI) is gradually shifting the paradigm of the entire drug development process, including regulatory writing and submissions, by offering faster and more efficient workflows. In this insightful review article published in Nature Medicine earlier this month, Daniel Ting and his team succinctly summarize the use of GenAI in medicine, including its evolution, current applications, and future opportunities. https://lnkd.in/eaZeEcgb #GenAI #DrugDevelopment #ArtificialIntelligence #RegulatoryAffairs #MedicalWriting #BioPharma
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AI in pharma……from fascination to function…… Tim Hardman, Founder and Managing Director at Niche Science & Technology Ltd, and one of the key minds behind the upcoming PCMG Clinical Outsourcing Community AI Symposium, explores the realities behind pharma’s AI fixation. Tim reflects on where AI has truly moved the needle, what lessons have been learned, and why success now depends less on hype and more on discipline: better validation, smarter procurement, and honest evaluation of impact. His perspective underpins one of the central aims of the PCMG AI Symposium, taking place on 24 November at the Royal Society of Medicine, London; to create a space where AI’s role in clinical development outsourcing can be discussed with nuance, balance, and practicality. From data innovation and governance to procurement and partnership models, the Symposium will bring together leaders from pharma, CROs, and service providers who are helping transform AI’s potential into tangible progress. Find out more about the PCMG AI Symposium: https://lnkd.in/gHHB7Art Tim Hardman, Varun Grover, MBA, Steve Martindill, Olena Goloborodko, David Davies, Pia Sauer Larsen, Leon van Wouwe #clinicalresearch #clinicaltrials #clinicaloperations #clinicaldevelopment #PCMG #AISymposium #AIinnovation #pharma
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