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Please make every effort to attend the keynote conversation. GenAI is a term that gets tossed around in our everyday vocabulary. But what does it really mean? And, how do you make it work for your organization? You will find out during this keynote. Then visit us at Booth #537 for further information. #GenAI #pharmacovigilance #drugsafety #patientsafetyfirst

Thrilled to attend #DIAEurope2024, where industry leaders converged to explore cutting-edge advancements in healthcare. From insightful discussions to impactful networking, the conference provided an invaluable platform to delve into the future of pharmaceuticals and regulatory affairs. Grateful for the enriching experiences and connections made! #HealthcareInnovation #Regulatory #clinicalresearch #clinicaltrial #gcp #pharmacovigilance #drugdiscovery #drugdevelopment #drugsafety

Join us for the 158th Real World Wednesday on December 11th at 11am EDT for a discussion with Gary Schneider, MSPH, ScD, founder of Delve-RW LLC, as we discuss his learnings from his organizations’ niche offering of conducting independent review of Statistical Analysis Plans (SAPs) for Pharma sponsored, regulatory agency committed, observational, non-interventional studies. You can join the conversation here: https://lnkd.in/gipkcPjH Gary Schneider, MSPH, ScD Matt Veatch Aaron Kamauu MD MS MPH Please check-out our website to join the club, get updates and see podcast recordings: https://rwd-rwe.club #isporeurope #realworlddata #rwd #realworldevidence #rwe #datascience #clinicalresearch #drugdevelopment #healthcareanalytics #clinicaltrials #drugdevelopment #medicalinformatics #EHR #electronichealthrecords #EMR #electronicmedicalrecords #operationaldefinitions #computableoperationaldefinitions #computablephenotypes #computablemeasures #measurelibrary #trialtokenization #triallinkage #augmentedtrials #datalinkage

Mastering the complexities of global clinical trials requires precise expertise and a strategic approach. At HiRO, we provide tailored solutions that span the entire drug development lifecycle—from discovery through to patient delivery. Our global experience, combined with profound local knowledge, empowers our clients to navigate regulatory landscapes confidently and achieve successful market entries. Discover how our dedicated partnership can transform your clinical development strategy. https://lnkd.in/dCpvXC7A #GlobalTrials #DrugDevelopment #ClinicalSuccess

How can we accelerate your clinical trial? Check out these 6 real-world examples to see our team in action.

More time for #patientoriented research with #realworlddata! There are #innovations and there are #innovators who drive progress. Often against resistance, but also hand in hand with what is. Two companies that have been doing this for a long time and have also ventured into new territory during the pandemic, have put their heads together again. DocMorris and DontBePatient Intelligence (DBPi) are taking the path of innovators and come from very different sides of the pharmaceutical supply chain. One from research and development, the other from patient care and pharmaceutical excellence. We have one thing in common: everything that is available in the pharmacy goes through clinical research, an immense amount of time, financial resources and, above all, reliable and well-founded findings from the reality of care. We have different ideas on how we can improve and accelerate this process, and it often makes sense to change perspectives and look for solutions together. We are staying tuned, and I would like to thank my colleagues at DocMorris for the open and solution-oriented discussion. Lars, Sonja, Oliver, Charlene, Timm, Hilke, Wolfgang, Julius, Francois, Elmar, Christoph, Kemal, Ute, Nicole, Sven, Silke, Paul, Catharina, Doris, Arnaud, Stéphanie, Silvia, Edgar, Thomas, Petra, Christina, Iris, Gregor, Ken, Simone, Simone, Nils, Nils, Zdenka, Christopher, Christophe, Andreas, Patrick #behindpatienteyes #patientengagement #patientcare #patientjourney #patientexperience

Day 1 of the Veeva R&D and Quality Summit in Boston did not disappoint! 🌟 One of the biggest takeaways was the growing focus on transforming safety from a compliance-driven task to a value-driven function. With advancements in GenAI and automation, the potential to leverage safety as a strategic asset is more real than ever. Moving beyond just meeting regulatory requirements, safety can now drive innovation, improve efficiency, and deliver better outcomes across the entire R&D process. Looking forward to seeing how this evolves and excited to be part of the journey! 🧬🚀 #VeevaSummit #RDSummit #Innovation #Pharma #Safety #ComplianceToValue" Let us know if you'd like to make any changes!

Need to fast-track custom collection kits or enhance visibility into sample tracking? Complex challenges call for a nimble approach. That’s why we are sharing 6 real-world examples of how we’ve helped clients accelerate drug development milestones with our agile approach. ⏱️ How can we accelerate your clinical trial? Download the case study to learn more. https://lnkd.in/g9fr2D7K #Nimble #DrugDevelopment #ClinicalMilestones #LabConnect

#Nimble #DrugDevelopment #ClinicalMilestones #LabConnect Need to fast-track custom collection kits or enhance visibility into sample tracking? Complex challenges call for a nimble approach. That’s why LabConnect is sharing 6 real-world examples of how we’ve helped clients accelerate drug development milestones with our agile approach. ⏱️ How can we accelerate your clinical trial? Download the case study to learn more: 👉 https://lnkd.in/g9fr2D7K

Whichever team you’re supporting in the Euro 2024 on Sunday - or if you’re avoiding it altogether - you can be sure that we'll be on your side when it comes to giving your drug its best shot at reaching the clinic. We promise end-to-end action with seamless support covering every aspect of non-clinical development and clinical oversight from a dedicated expert team who are ready to hit the ground running in days. We’ll help you keep on side with the regulators to avoid unnecessary holdups - and you can trust us not to drop the ball on any of the details. With more than 160 programmes delivered to date, we’re proven winners with an impressive track record of getting drugs into and through the clinic. It’s never too early to start thinking about how you’ll get your drug to and through clinical trials. Whatever stage you’re at - from spin-out to start-up to established biotech - get in touch with Jonathan Kearsey to find out how we can help: jkearsey@leadstodevelopment.com #drugdevelopment #clinicaltrials #biotech