7 days to go! Brace yourselves for an engaging discussion on Europe's position in global clinical trials. Join us and Xtalks on November 29 for a webinar dissecting the implications of CTIS and Regulation 536/2014. Save your spot! Register here: https://zurl.co/UnFn #ClinicalTrials #RegulatoryUpdates #ClinicalResearch #GCPServiceInternational #Webinar #UpcomingWebinar
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Understanding Clinical Trial Protocol - part 2 https://lnkd.in/dtijNAa8
Understanding the Basics of Clinical Trial Protocol (Part 2)
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View this short webinar to learn how CROs can tap into best practices for mitigating risk & addressing specific clinical supply challenges commonly associated with adaptive, decentralized, platform & other complex trial designs. https://ow.ly/nWjP50Q5Eyq
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🔍 Exciting News Alert! 📢 Following the latest MDCG CIE meeting, a new guidance on the content of clinical investigation plan (=protocol) has just been released, along with an informative appendix. Dive into the details here: https://lnkd.in/eJhUU7z9 This comprehensive guidance promises to streamline the process of requesting authorization for clinical investigation by outlining clear expectations. Stay tuned for another upcoming guidance focusing on the content of the investigator brochure! 📑 #ClinicalResearch #MedicalDevices #RegulatoryUpdates
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From 700 to 60 hours - revolutionize your proposal creation with CTB 🕒 Discover the future of clinical trial efficiency
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In the world of clinical trials, quality and compliance are paramount. Yet, many CROs still grapple with quality concerns, leading to regulatory issues and increased costs. Discover the power of Systemic Root Cause Analysis (RCA) in our latest whitepaper. Dive into the importance of uncovering the root causes behind non-compliance, and how it can revolutionize your approach to clinical research. Join ZENOVEL, as we explore the regulatory perspective, the significance of thorough investigations, and the journey toward enhanced efficiency and patient safety. Read the full whitepaper to stay at the forefront of clinical trial excellence https://lnkd.in/g4vJVRnh #ClinicalTrials #ClinicalResearch #QualityAssurance #RootCauseAnalysis
ROOT CAUSE ANALYSIS IN CLINICAL RESEARCH
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#PartIII Unlocking the Power of Post-Trial Documentation in Clinical Studies! 📑✨ Join us as we dive into the pivotal role of essential documents after the conclusion of a clinical trial. Discover how meticulous documentation seals the integrity of trial results and ensures compliance with regulatory standards. Stay informed, stay compliant. Read more about this topic here: https://zurl.co/ZnNw Watch the complete video: https://zurl.co/IWpe #ClinicalTrials #TMF #DocumentationExcellence #ClinicalResearch
The Basics of Essential Documents in the Trial Master File – Part 3 - After the Clinical Phase
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View this short webinar to learn how CROs can tap into best practices for mitigating risk & addressing specific clinical supply challenges commonly associated with adaptive, decentralized, platform & other complex trial designs. https://ow.ly/nWjP50Q5Eyq
Webinar: Advanced Clinical Supply Strategies for Decentralized and Other Complex Study Protocols
catalent.voicestorm.com
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View this short webinar to learn how CROs can tap into best practices for mitigating risk & addressing specific clinical supply challenges commonly associated with adaptive, decentralized, platform & other complex trial designs. https://ow.ly/nWjP50Q5Eyq
Webinar: Advanced Clinical Supply Strategies for Decentralized and Other Complex Study Protocols
catalent.voicestorm.com
To view or add a comment, sign in
-
View this short webinar to learn how CROs can tap into best practices for mitigating risk & addressing specific clinical supply challenges commonly associated with adaptive, decentralized, platform & other complex trial designs. https://ow.ly/nWjP50Q5Eyq
Webinar: Advanced Clinical Supply Strategies for Decentralized and Other Complex Study Protocols
catalent.voicestorm.com
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