IDDI - Regulatory Statistics & Clinical Data Science Experts’ Post

Come meet Tara Kervin and I at #PCTSummit in Boston May 6-7! We will be at booth #11 ready to discuss how we can partner with you to resolve your clinical trial needs. Schedule a meeting: https://lnkd.in/gJe-6qJj #PCTSummit #biometricscro #clinicaltrials #biostatistics #datamanagement #lifesciences #trialdesign #IDDI

Attending #OCTNewEngland November 1st - 2nd? Meet with our team at booth #28 to discuss the current challenges we face in the clinical trial landscape and how we can adapt together. #OutsourcingInClinicalTrials #ClinicalTrials #LifeSciences #ClinChoice #ClinChoiceCanHelp #ContractResearchOrganization

Episode 18 out now! Have you ever used the International Index of Erectile Function (EF) Domain Score in your Clinical Trials? Planning a Clinical Trial? connect with us to receive your complimentary Study Outline - connect@vediclifesciences.com #clinicaltrials #questionnaire #goldstandard #tools #clinicalresearch #biomarkers

It is a dreary morning 🌧 here in NC but we are ready for #PCTSummit in Boston! We are excited to connect with industry leaders and discuss the clinical trial obstacles you've encountered and how we can help you overcome them. See you soon! Visit Tara Kervin and I at Booth #11 #riskmitigation #regulatorystatistics #clinicaldatascience #biostatistics #datamanagement #trialdesign #consultancy #IDDI

For an early-stage #biotech data readouts carry big risks and potential rewards. Whether providing proof of concept, proving safety and tolerability, or clearing the way for final regulatory approval, clinical trial readouts are critical de-risking events. Communicating a clear, consistent message to your audiences is crucial to success, no matter what the data show. Read my step-by-step guide in MedCity News on how to effectively leverage clinical trial readouts. bit.ly/3SzSdJC

MEDIN has been operational for 16 years and during the creation of the next MEDIN Business Plan, we took the time to reflect on some key milestones. From an initial group of four Data Archive Centres sharing 800 datasets in 2010 to a mature network that shares over 17,500 datasets owned or managed by more than 600 different organisations across sectors in 2023, is a remarkable feat. MEDIN’s aspirational and ambitious new 5-year business plan builds upon the successes of the past and will see MEDIN strengthen its position as an internationally-recognised authority on marine data management. By setting out a framework of strategic goals and deliverable activities, this plan captures MEDIN’s objectives and aspirations for its next half-decade. Find out more about the MEDIN Business Plan 👇https://hubs.ly/Q02BgQtm0 #MEDINBusinessPlan2429 #marinedatasharing

Don't miss the latest episode of Molecule to Market with Helen Shaw and Dan Henley, co-founders of VCTC, a UK clinical trial site that specializes in delivering virtual and decentralized clinical trials.!🎙️ In this episode, they discuss: 👉 How the frustrations of being a patient with an orphan disease shaped the ethos of VCTC 👉 The uptake of patient recruitment and retention in virtual and decentralized clinical trials 👉 Finding a powerful niche in the life sciences space to enable you to grow, globally Listen below! You don't want to miss it ⬇️ #PharmaPodcast #CDMO #LifeSciences

Clinical trials NEED innovation. Is Advarra the one to guide the way? Gadi Saarony, CEO of Advarra, discusses the future of clinical research in our latest BioBreakthroughs with host Jared S. Taylor. Tune in to learn about Advarra's innovative approaches in clinical trials. #ClinicalResearch #AdvarraInnovation #sohcpodcasts #HealthcareInnovation Full length video in the comments!

The edition 04 of my newsletter CLINICAL OPERATIONS SPOTLIGHT discusses the Regulatory Framework for ATMPs 💊 🗝 KEY REGULATORY CHALLENGES include: -         Regulatory differences across countries -         Early biomarker response -         Non-clinical studies -         Lack of adequate animal models -         Regulatory requirements for site selection The newsletter discusses challenges but also the related impact and potential solutions. Also, references are indicated for further reading. 📅UPCOMING EVENTS - Want to learn more about Clinical Trials with ATMPs? Check out my upcoming training on 14-15 March 2024 with the FORUM Institut für Management GmbH Institute for Management - You are interested how to collaborate in a remote team? Join me for a Clivolution webinar on virtual teams on 21 March 2024 at 01:00 pm - Meet me at the Clinical Trials Strategic Summit by Agile Falcon Strategic Group LLC. in Munich on 28-29 May 2024 #ClinicalTrials #CellAndGeneTherapy #RegulatoryFramework Clinical Excellence GmbH

To prioritize patients in #clinicaltrials, a CRO #centrallab should provide tools and systems that oversee all trial aspects, sharing real-time data with project teams for informed decisions, especially in complex trials. In this recent webinar, our experts Chris Clendening, Olivia Aspite, Tricia Moloy (Abbott) and Tracy Roe explain how PPD® Laboratory services are changing the central lab paradigm to make studies more efficient. » https://bit.ly/48YPErV