Battelle Health

🏭 The future of #pharmamanufacturing is #agile. Learn how continuous processing, modular equipment, and AI bring speed and flexibility to drug manufacturing. Learn more: https://okt.to/NofnCv #AgilePharma #TechInPharma

Streamline your g-DDCP development process. This white paper introduces a simplified six-phase design assessment process that fosters innovation, reduces development time and costs, and streamlines regulatory approval while ensuring safety and effectiveness. Download now to explore the possibilities and gain detailed insights. 𝗪𝗵𝗮𝘁 𝗬𝗼𝘂'𝗹𝗹 𝗟𝗲𝗮𝗿𝗻: - A Six-Phase Alternative Assessment Method - Strategies to reduce dependence on comparative use #humanfactors (cuHF) studies - How to encourage innovation in #MedicalDevice design while reducing regulatory burden - Tips to improve your regulatory filing quality Download the white paper today: https://okt.to/qwLJyW

The medical device industry is no exception to the advent of artificial intelligence. This Inside Battelle blog illustrates how AI technologies evolved throughout the years, how Battelle used (and is using) machine learning (ML) and AI to develop life-changing medical devices, and how to responsibly advance medical device innovation in the "AI Age".

Ready to take an active role in Partnership for Quality Measurement (PQM) committee activities? Participating in the Endorsement and Maintenance (E&M) or Pre-Rulemaking Measure Review (PRMR)/Measure Set Review (MSR) committees offers you the opportunity to: ⚕️Influence Health Care Quality: Play a pivotal role in shaping the standards and measures that impact health care quality and patient outcomes.  🗣️ Collaborate with Experts: Work alongside a diverse group of professionals and experts, fostering innovation and sharing knowledge.  ➕ Enhance Your Professional Growth: Gain valuable experience and insights into the health care measurement process, enhancing your professional development and network. Submit your nomination by May 15: https://lnkd.in/eQquW85v #healthcare #qualitymeasurement #qualityimprovement #volunteer #makeadifference #professionaldevelopment #patientcare

Generic drug-device combination products (g-DDCPs) play a vital role in the #healthcare market. Our new, simplified design assessment process could reduce development time and costs associated with #regulatorycompliance while encouraging device innovation. Dive into our white paper to learn more: https://okt.to/A6CVwS 𝗪𝗵𝗮𝘁 𝗬𝗼𝘂'𝗹𝗹 𝗟𝗲𝗮𝗿𝗻: - A Six-Phase Alternative Assessment Method - Strategies to reduce dependence on comparative use #humanfactors (cuHF) studies - How to encourage innovation in #MedicalDevice design while reducing regulatory burden - Tips to improve your regulatory filing quality #HumanCenteredDesign

The medical device industry is no exception to the advent of artificial intelligence. This Inside Battelle blog illustrates how AI technologies evolved throughout the years, how Battelle used (and is using) machine learning (ML) and AI to develop life-changing medical devices, and how to responsibly advance medical device innovation in the "AI Age". https://okt.to/4Reth5

Headed to #JPM2025? Schedule time to connect with Andre LaFreniere, Breck Petrillo, or Chris Kocheran to learn how Battelle can support your #healthcare initiatives from concept to commercialization. https://okt.to/XWpIne

#ForeverChemicals have properties that are useful, but they can contaminate our environment and pose health risks. Check out this Inside Battelle blog to learn more. https://okt.to/9d0joM

Looking for expert #HumanCenteredDesign insights to enhance your #medicaldevice? Connect with Brianne Pragg, Ph.D. Brianne is a Human Factors Engineer with over 11 years of experience in human subjects research. Her expertise includes research design and methodology, data collection and analysis, and study execution. Her PhD is in sociology and demography, and she has experience in statistics for behavioral sciences. From initial client meetings to presenting results, Brianne is involved in every phase of the assessment process. Her responsibilities include study planning, protocol development, coordinating recruitment, managing IRB submissions and approvals, conducting risk analyses, and overseeing study execution. She has extensive experience moderating studies ranging from contextual research to usability studies. As the principal investigator on several critical research programs, she has been instrumental in validating over-the-counter products and supporting FDA applications for prescription devices. Interested in learning more? Contact our team to explore how to collaborate to innovate and improve user experiences. https://okt.to/0PyUNX

A significant challenge in gene therapy delivery has been limitations in cargo capacity of the gene payload carrier. In this episode of Supplier Horizons, host Tom von Gunden talks with technical director Gabe Meister and scientist Anthony Duong from Battelle about the promise of polymer nanoparticles as delivery vehicles for treating rare diseases with in vivo gene therapies. Watch it here: https://lnkd.in/emBKgEw6