From breakthrough drug discovery to next-gen clinical trials, AI and ML are driving unprecedented change across the life sciences industry. But what’s coming in 2025? In this must-read article, IQVIA’s Alison Sloane joins fellow industry experts to share her predictions on how AI will shape healthcare innovation in the year ahead. Read the full article here: https://bit.ly/3Y0oCwm #AIinHealthcare #LifeSciences #HealthTech
IQVIA Safety & Regulatory Compliance
医院和医疗保健
Danbury and Durham，Connecticut and North Carolina 20,864 位关注者
End-to-end integrated tech services and analytics solutions for safety, regulatory, quality and commercial compliance
关于我们
IQVIA has a vision that goes beyond simply optimizing individual safety, regulatory, quality, and compliance functions. Using cloud-based technology combined with advanced analytics—including artificial intelligence and machine learning—IQVIA is bringing together global regulatory intelligence, safety data, product quality information and legal/ethical guidance on an integrated platform. For customers, this means: ? Improved compliance performance at lower cost across all functions ? Visibility across their complete compliance landscape ? Faster response times ? More predictive planning, throughout the product lifecycle Learn more are: www.iqvia.com/GlobalCompliance
- 网站
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https://www.iqvia.com/GlobalCompliance
IQVIA Safety & Regulatory Compliance的外部链接
- 所属行业
- 医院和医疗保健
- 规模
- 超过 10,001 人
- 总部
- Danbury and Durham，Connecticut and North Carolina
- 领域
- commercial compliance、safety compliance、regulatory compliance、quality compliance和compliance
动态
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From intelligent chatbots to self-service portals, AI is transforming how healthcare providers and patients access critical information. By handling routine queries, these innovations take the pressure off medical information teams – freeing time to focus on more meaningful, high-value interactions. Discover how AI is reshaping the MI landscape in this fascinating piece from IQVIA’s Simon Johns: https://bit.ly/4kH6RMv #AIinHealthcare #MedicalInformation #DigitalHealth
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Transferring marketing authorizations can be a complex, high-stakes process – but with the right strategy, it doesn’t have to be. Regulatory Affairs and Drug Development Solutions (RADDS) streamline MAT, ensuring compliance, reducing risks, and keeping transitions seamless. Discover how our expert-led approach can help you manage global MATs with efficiency, speed, and confidence. https://bit.ly/4hBmK45 #RegulatoryExcellence #PharmaCompliance #MarketAccess
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With over 3,000 safety professionals in more than 100 countries, our flexible drug safety system allows you to improve quality, reduce costs, and access data for every phase of the safety lifecycle. From real-time adverse event detection to robust reporting features, you can stay one step ahead in safeguarding patient outcomes with IQVIA Vigilance Platform. Find out more: https://bit.ly/3FMqmD6 #Pharmacovigilance #DrugSafety #PatientProtection
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How do small and mid-sized MedTech companies digitize QMS and adopt AI—despite limited resources? In the first of our three-part blog series, subject matter experts share their unique perspectives on the specific challenges of Quality Management System (QMS) digitization and AI adoption for SMEs—from resource constraints to the multi-hat roles of QA/RA professionals. Get an inside look at what a typical QMS setup entails, and learn how to future-proof your SME operations: https://bit.ly/3DIw6xf #MedTech #QMSDigitization #AIinHealthcare
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Navigating your product’s post-approval phase can be challenging—but it doesn’t have to be. Our latest article reveals three crucial steps for a resilient regulatory strategy, even when you’re juggling multiple markets, renewals, and labeling updates. Discover how AI and big data analytics help you stay ahead of shifting regulations, streamline decision-making, and reduce administrative burdens. Ready to make post-approval your competitive advantage? Read Marcela Mi?o's expert insights: https://bit.ly/4kveTYH #RegulatoryStrategy #PharmaCompliance #AIinPharma
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Elevate your PV strategy with IQVIA Vigilance Platform – a comprehensive SaaS solution designed to simplify data capture, boost operational efficiency, and ensure robust compliance. By automating manual tasks and integrating real-time data, you can focus on what truly matters – improving patient safety and enhancing your product’s risk profile. Explore how IQVIA Vigilance Platform can transform the way you manage risk and ensure compliance: https://bit.ly/4buMa26 #DrugSafety #Pharmacovigilance #PatientSafety
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We are thrilled to announce that Cynthia Verst, PharmD, President of Design & Delivery Innovation at IQVIA, will be moderating a panel discussion at the DIA 2025 European Annual Meeting in Basel, Switzerland. ? Join us on March 18, 2025, as Cynthia leads a distinguished group of experts in exploring new paradigms for utilizing AI across the medical product development continuum. This session will emphasize the importance of training, workflow alignment, change management, and continuous improvement for the industry; early engagement with regulators; and the need for transparency, trust, and incorporating the patient voice. ? Don't miss this opportunity to gain valuable insights from leaders in the field and learn how AI is transforming healthcare. ? https://lnkd.in/dEMa2gRv ? #DIAEurope2025 #AIinHealthcare #ClinicalTrials #PatientEngagement
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Reaching the post-approval phase is a significant milestone for pharma companies, but it comes with its own set of challenges. IQVIA’s Marcela Mi?o, Global Head of Lifecycle Management for Marketed Products, shares insights on effective post-approval lifecycle management. Discover how planning, communication, and leveraging cutting-edge technologies can drive commercial success. Read the full article to learn more: https://bit.ly/3DHgEBr #PharmaLifecycle #PostApprovalSuccess #IQVIAInsights
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As the pharmaceutical industry evolves, the demand for accurate and accessible Medical Information is at an all-time high In our latest Deep Dive in Pharmaphorum, Simon Johns explores how AI-powered solutions are revolutionizing MI services, enhancing compliance, and building trust across the healthcare ecosystem. Discover how automation, AI, and machine learning are streamlining complex MI requests and empowering customers through self-service portals and chatbots. Read now for expert insights: https://bit.ly/4iOfmDx #MedicalInformation #MedicalAffairs #MI #HealthcareCompliance
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