WEBINAR 10.10.24 | Maximize Control and Transparency on the Path to Study Go-Live. Join us on October 10th to learn how Medable, Inc's platform, Medable Studio, can streamline clinical trials. Discover how to accelerate study start dates, improve data accuracy, and cut costs by using a pre-built assessment library. The session includes a live demo showcasing Medable Studio's capabilities to enhance study efficiency, transparency, and control! Secure your spot today: https://lnkd.in/deXHMWqg
Clinical Leader
Pharmaceutical Manufacturing
Erie, Pennsylvania 15,228 followers
A resource and forum to investigate and resolve the common struggles related to running effective clinical trials.
About us
The landscape of the life sciences industry is as vast and varied as the professionals who work in it. Some online resources aim to serve the entire space. We wish them luck. Instead, our goal is to be the most valuable resource for a specific segment of the industry – clinical research & trials – and the professionals who make their living there. The Clinical Leader community is not made up of generalists. They’re specialists, like us. We deliver in-depth content from authoritative authors and sources because that’s what our community demands. Our editors connect with and interview top clinical executives from pharmaceutical and biotech companies who share best practices, challenges faced and overcome, clinical trends, partnering strategies, and experiences implementing new technologies. Additionally, our Clinical Leader Live series of live events provides an interactive forum where sponsor companies talk about some of today's biggest challenges when managing clinical trials. Even better, the audience gets to ask questions during the presentation.
- Website
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https://www.clinicalleader.com/
External link for Clinical Leader
- Industry
- Pharmaceutical Manufacturing
- Company size
- 51-200 employees
- Headquarters
- Erie, Pennsylvania
- Founded
- 1995
- Specialties
- Clinical Trials and CRO
Updates
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What Is A LIMS, And How Do You Know If You Need One? Consider these key factors when deciding if your team needs a Laboratory Information Management System (LIMS) and explore steps to optimize your biopharmaceutical development processes. https://lnkd.in/emFRE7m5 By Claire Hill and Dana Vanderwall, ProPharma
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In part two of this series on individual patient data return (iPDR), Legacy Health Strategies experts offer four steps to help sponsors make iPDR a reality: https://lnkd.in/e37DrtVe By Jessica Scott M.D., J.D., MD, JD, CEO, and Jennifer Millman, JD, senior director of strategy and operations, Legacy Health Strategies
4 Steps To Help Sponsors Return Individual Patient Data
clinicalleader.com
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How Can We Improve/Simplify the Clinical Trial Digital Dataflow? Join our next Clinical Leader Live event on October 31st, where our expert panel will discuss the advantages of improving and simplifying the dataflow of clinical trials, as well as the challenges associated with creating a connected digital dataflow — including digital health channels — that spans from protocol to data collection to CSR. 📌 Reserve your spot for the digital discussion: https://lnkd.in/eTyNS2Tz
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WEBINAR TOMORROW! Don't miss our discussion with Medable, Inc on how to accelerate study start dates, improve data accuracy, and cut costs by using a pre-built assessment library. The session includes a live demo showcasing the capabilities of Medable Studio to enhance study efficiency, transparency, and control. 🔐 Secure your spot today: https://lnkd.in/eGg-TRXU
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Brian H. Johnson,Ph.D., Ph.D., VP, R&D Technology at Takeda discussed with Chief Editor Dan Schell the huge opportunity of connecting disparate ClinOps data and leveraging generative AI to reduce costs and labor during the clinical process. Read their discussion here: https://lnkd.in/ev6hg7qg
AI Can't Help Bad ClinOps/Health Equity Data
clinicalleader.com
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WEBINAR TOMORROW! This discussion on 10/8 will review some key challenges facing medical writing submission specialists today and reveal the medical writing strategies that can lay a foundation for success each and every time. 🔐 Secure your spot here: https://lnkd.in/eYPcSga7 🗣 Speakers: Kelly Kilibarda, PhD, Associate Director of Medical Writing, inSeption Group Robin Johnson, PharmD, PharmD, Senior Medical Writer, inSeption Group Sara Symons, Director of Medical Writing, inSeption Group
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In this week's issue, we'll explore how adherence to GCP influences site feasibility, what’s good and bad regarding the new FDA Guidance on diversity, why we must include people with disabilities in clinical trials, how to prioritize patient safety in CAR-T therapy, and other popular insights! Donatella Ballerini | Dan Schell, Stacey Bledsoe, Garo Kiledjian, Denise N. Bronner, Ph.D. | Richie Kahn, Canary Advisors® | Cerba Research | Christina Brennan, MD, Northwell Health | Kate Yawman, Advarra | Marcio Souza, Praxis Precision Medicines, Inc. | OpenClinica | Greenphire
Why Sponsors Must Check For Site GCP Adherence During Feasibility Studies, What's Good And Bad About The FDA's Diversity Guidance, and More
Clinical Leader on LinkedIn
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Are there some pools of diverse patients — including disabled patients — that we as an industry tend to overlook, but that could be great for clinical trial recruiting? Garo Kiledjian of the SGM Alliance says yes, and he gives some examples. https://lnkd.in/enycAry9
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Stay ahead in drug safety by mastering the use of Periodic Safety Update Reports (PSURs) and their evolution into Periodic Benefit-Risk Evaluation Reports (PBRERs) to ensure ongoing public health protection. https://lnkd.in/en7gPHeF Source: ProPharma
Understanding The PSUR And PBRER
clinicalleader.com