This is your chance to claim your FREE pass to BioProcess International Fall & Viral Vectors Digital Week! Book your free pass today. Join us for an exclusive webinar series from December 2-4, 2024, to stay at the forefront of innovation in viral vector development. This series offers the latest advancements in analytical methods, process development, and manufacturing platforms, aimed at reducing costs, enhancing quality, and accelerating your products to market. Gain valuable insights into scientific innovations that drive efficiency across critical areas, including process development, cell line optimization, upstream and downstream processing, and manufacturing strategy. Don’t miss this opportunity to elevate your expertise and take your viral vector products to the next level. From the comfort of your own home, office, or anywhere else, you can enjoy our fantastic line up from Bioprocess experts who will share their latest insights. Book Now to Claim your Complimentary Free Pass - https://bit.ly/48BtEUb

Clinical Data Disclosure, Transparency and Plain Language Summaries is just over 3 months away! Will you be attending? Use the link in the event details below to learn more and book your spot.

🚨 CALLING ALL TRADE AND CHANNEL PROFESSIONALS 🚨 📢 Rates are going up and your last chance to join hundreds of your peers at a discounted rate expires FRIDAY! What can you expect? 💡40+ industry experts ready to collaborate and share their expertise  💡35 robust sessions including breakouts, workshops, tracks and more for a customized event experience 💡7+ networking hours with multi-stakeholders across the trade community 💡1 choice for trade excellence to accelerate market access ✅ Download the full agenda and book by November 15th to save $200: https://lnkd.in/eRXEFzwg #TRADE2024

Want to know how to elevate your clinical trial logistics, reduce site and patient burden, and maximise participant retention? Global Clinical Trials: Clinical Operations Digital Day is here to help! Featuring 2 presentations from Moderna and Medable, Inc plus live Q&As, this free-to-attend expert led webcast series on 4th December will equip you with lots of new ideas to maximize your clinical operations strategy.   🎥Webcast: The quiet champion accelerating trial success 10am EST / 3pm GMT / 4pm CET  Discover practical strategies to boost participant retention and accelerate clinical trial success in this interactive session, featuring real-world insights on digital tools, decentralized methods, and operational enhancements from experts at the forefront of retention strategy. - Mindy Gruba, M.P.H., Associate Director Patient Centricity, Moderna - Kelsey O'Brien, MPH, ALM, CCRP, Clinical Operations, Infectious Disease, Moderna   🎥Reducing the site and patient burden through excellence in trial logistics 11am EST / 4pm GMT / 5pm CET Explore the latest strategies and innovations for managing clinical trial operations with a focus on device provisioning and data workflows. And, discover how leading organisations are using cutting-edge logistics solutions to streamline supply chain management, optimize data collection, and improve participant satisfaction. - Jena Daniels, VP Patient Success, Medable - Asad Khan, Alliance Director, Medable Register now: https://lnkd.in/eAMaK6Vp #ClinicalTrials #ClinicalOperations #ClinicalResearch #ClinicalLogistics #ClinicalTechnology #ClinicalData #PatientCentricity #ClinicalSites #PatientRetention #DecentralizedTrials

Don’t miss out on the Antibody Engineering & Therapeutics US conference this December 15-18 in San Diego, final savings end on Friday. With 950+ industry leaders, top pharma, and cutting-edge research all in one place, this is the event you need to be at. See who’s attending and download the attendee list to discover who you could be connecting with. 💸 Plus, book by Friday, November 15, to save $200 on your pass! Book your pass: https://lnkd.in/dFb92Cm 🔗 Download the attendee list: https://lnkd.in/eaUQmjHy #AET2024 #AntibodyEngineering #NextGenAntibodies

TIDES Europe Keynote Sessions have begun! We’ve got a full house ready to learn more about…. 🧪 Discovery of RNA - modifying Ribozumes by Takumi Okuda, PhD of University of Würzburg ❓How Novo Nordisk is expanding their technology platforms via strategic internal and external investments by Karina Thorn of Novo Nordisk ✍️ Designing the once-weekly and oral GLP-Semaglutide by Jesper Lau of Novo Nordisk This afternoon, look out for more keynote sessions from industry experts! #TIDESEUROPE

How can refining trial logistics and leveraging advanced technologies help you streamline processes, enhance data accuracy and simplify the experience for clinical sites and patients alike? Join Medable, Inc’s Jena Daniels, VP Patient Success and Asad Khan, Alliance Director online on 4th December to find out in this complimentary webcast exploring the latest strategies and innovations for managing clinical trial operations with a focus on device provisioning and data workflows. Webcast: Reducing the site and patient burden through excellence in trial logistics  11am EST / 4pm GMT / 5pm CET - Best practices for managing device deployment and achieving a 99% on-time device shipping rate. - How to ensure data integrity while navigating the complexities of global supply chains. - Strategies for unlocking new patient populations and improving patient experience in digital and hybrid trials. - Innovative approaches to reduce delays and streamline the logistics of clinical trials, enhancing overall site efficiency. Discover how leading organizations are using cutting-edge logistics solutions to streamline supply chain management, optimize data collection, and improve participant satisfaction. Register now: https://lnkd.in/eGAX_R9w #ClinicalTrials #ClinicalOperations #ClinicalResearch #ClinicalLogistics #ClinicalTechnology #ClinicalData #PatientCentricity #ClinicalSites

Guten Morgen from Germany! 🇩🇪 TIDES Europe workshops have kicked off this morning 🧪 With workshops focusing on: 🧬 Synthesis, CMC and Characterization of Long and Complex Oligonucleotides 🧬 Unlocking Insights: CMC, Quality & Regulatory 🧬 Peptide Therapeutics 2.0: Design and Properties of New and Improved Peptides This year we’re expecting 650+ total attendees! We’re excited to share updates about our event this year from the beautiful city of Hamburg. If you are attending, don’t forget, we have the TIDE Turner game! Participate for a chance to win an iPad, Airpods, or an Amazon gift card! Questions? Visit us at the registration desk. #TIDESEUROPE #Oligo #Peptide #mRNA #conference

Want to improve participant retention for your clinical trials?    Join Moderna’s Mindy Gruba, M.P.H., Associate Director Patient Centricity and Kelsey O'Brien, MPH, ALM, CCRP, Clinical Trial Manager, Clinical Operations, Infectious Disease online on 4th December for new ideas and inspiration on how to do it in this complimentary webcast!   Webcast: The quiet champion accelerating trial success   10am EST / 3pm GMT / 4pm CET     Participant retention is a clinical trial’s quiet champion—it ensures participant safety, powers the trial, and maximize resources—accelerating trial success.   In this interactive session, we'll break away from the typical retention talk by diving into real-world experiences from those who are at the forefront of retention monitoring, strategy, and implementation.   You’ll not only hear about the challenges, but also explore solutions that have shown promise— digital tools, decentralized approaches, and operational enhancements.   Prepare yourself for a candid, practical perspective on tackling retention in today’s trials.    Register now: https://lnkd.in/gKKx86GM   #ClinicalTrials #ClinicalOperations #ClinicalResearch #PatientRetention #DecentralizedTrials

Want to get a better understanding of clinical evidence for medical devices? Join Shelley Jambresic, Senior Clinical Evaluation Manager at Geistlich Pharma AG next week in Module 11 of this year’s Medical Device School live online training course, where she will walk you through: - Clinical evidence and your medical device  - The impact of the MDR on clinical evidence requirements  - Clinical Evaluations and Clinical Investigations - Utilising real world evidence - How clinical evidence links to risk management, biocompatibility, PMS - Involving clinical evaluators throughout medical device lifecycle   Learn more about all of the 18 modules within this year’s Medical Device School agenda and discover how you and your colleagues can benefit. View the full agenda: https://lnkd.in/e9yPg9vV Register today: https://lnkd.in/ebt36ZuM #MedicalDeviceSchool #MedTech #MedicalDeviceRegulations #EUMDR #MDR #MedicalDevice #MedicalDevices #RegulatoryAffairs #ClinicalEvidence #ClinicalEvaluations