We’re 20 days away from the start of Veeva Summit: R&D and Quality and the fme team couldn’t be more excited. This is one of the biggest events of the year to discover the trends shaping the future of R&D and quality, as well as innovations in clinical, quality and manufacturing, regulatory and IT. Read below to learn more about Veeva Summit and why fme is a certified Veeva partner and Gold sponsor of this exciting 2 day event! #VeevaSummit #biopharma
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🚀 Accelerate Your Clinical and Commercial Success with Veeva Vault 24R2! 🚀 Last week, we dived into the world of Regulatory and Safety with Veeva Vault 24R2. This week, we're turning our focus to the heart of your operations: Clinical and Commercial. Discover how the latest advancements in Veeva Vault can streamline your clinical trials, enhance commercial operations, and drive better patient outcomes. From accelerated clinical development to optimized commercial strategies, 24R2 offers the tools you need to succeed. But that’s not all! Next week, we’ll dive deep into the most anticipated platform features of Veeva Vault 24R2. Stay tuned for more insights and best practices! #VeevaVault #24R2 #ClinicalTrials #CommercialOperations #LifeSciences #Pharma #Biotech #Innovation #WolvioSolutions
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Associate Director - Business Development @Cencora PharmaLex New Business Strategy planning I Client Partnership I Solution design expert I Vendor Management I M&A I Pharmaceutical, Biotech & Medical Device client base
#Cencora #PharmaLex welcomes - psiXchange3.0 🔊 - Automating the end-to-end distribution, tracking, and acknowledgment process of vital clinical trial safety documents to various stakeholders across different countries. - Offers flexible delivery and pricing options tailored to biopharmaceutical companies and CROs of all sizes. - Utilizing the psiQ "brain," a regulatory intelligence database updated by global PV experts, customizable for 55 countries and expanding. - User-friendly portal facilitates real-time access to safety reports, enabling proactive management. It includes a library of Investigator Brochures, simplifying risk comprehension and enhancing patient safety. - Supports third-party submissions with automated preparation and tracking, reducing time and compliance risks.
Cencora PharmaLex is thrilled to introduce psiXchange 3.0, our latest intelligent and automated clinical trial safety reporting software 🚀 Discover how psiXchange 3.0 is revolutionizing safety reporting processes, providing intelligent automation and streamlining clinical trial safety reporting like never before. Read more about this groundbreaking innovation: 🔗 https://lnkd.in/dxMwifbQ #CencoraPharmalex #psiXchange #ClinicalTrial #SafetyReporting #Innovation #PharmaceuticalIndustry
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Looking to minimize manual paperwork in your #CVQ tasks? 📝 Mark your calendar for Saurabh's upcoming webinar, where he'll guide you through the world of #digitalCQV 💻 Learn how it's reshaping conventional practices and paving the way for Pharma 4.0. Can't miss it! 👉 https://lnkd.in/dB2V7cMA
Digital CQV and Pharma 4.0: Paving the Way for Future Success - ValGenesis
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Did you know that there is a cloud-based tool that can validate life sciences companies’ systems, procedures, and equipment up to five times faster than the current paperwork method? FIVE Validation is another Start Up that we've highlighted in our CPHI Disruptor Watchlist. Their solution, called GO!FIVE®, is a SaaS platform that accelerates validation studies by over 5x compared to traditional methods. FIVE Validation specialises in validation processes for businesses operating in regulated industries, such as the biopharmaceuticals and medical sectors. It offers expertise in ensuring compliance with regulatory bodies like the FDA, ICH, and EMA while optimising operational efficiency. FIVE Validation’s services aim to minimise risks associated with products and services by streamlining processes through electronic documentation, replacing traditional paper-based systems. FIVE Validation’s CEO, Silvia Martins, explained a bit more about their regulatory process in our interview with them: “FIVE Validation's SaaS solution meets EMA/FDA standards, and users leverage pre-ready validations for accelerated processes in Life Sciences.” See our CPHI Disruptor Watchlist at https://lnkd.in/eTv2T2xz to learn about other innovative Start Ups disrupting the pharma space.
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Unlock the full potential of Veeva Vault RIM! Discover tips to optimize regulatory processes and ensure efficiency in our blog.
Staying ahead of regulatory requirements in the biotech and pharma industries means being agile and detail-oriented. Explore our blog to see how Veeva Vault RIM can transform your regulatory processes for greater compliance and efficiency. Discover how to streamline workflows, harness advanced reporting, and optimize your Vault RIM environment for maximum performance. Find out more: https://lnkd.in/e87GXjF4.
Honing Your Vault RIMS Environment for Peak Performance
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Streamline regulatory compliance with Veeva Vault RIM! Learn how to enhance workflows and optimize performance in our blog.
Staying ahead of regulatory requirements in the biotech and pharma industries means being agile and detail-oriented. Explore our blog to see how Veeva Vault RIM can transform your regulatory processes for greater compliance and efficiency. Discover how to streamline workflows, harness advanced reporting, and optimize your Vault RIM environment for maximum performance. Find out more: https://lnkd.in/e87GXjF4.
Honing Your Vault RIMS Environment for Peak Performance
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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!
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Staying ahead of regulatory requirements in the biotech and pharma industries means being agile and detail-oriented. Explore our blog to see how Veeva Vault RIM can transform your regulatory processes for greater compliance and efficiency. Discover how to streamline workflows, harness advanced reporting, and optimize your Vault RIM environment for maximum performance. Find out more: https://lnkd.in/e87GXjF4.
Honing Your Vault RIMS Environment for Peak Performance
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Streamline regulatory compliance with Veeva Vault RIM! Learn how to enhance workflows and optimize performance in our blog.
Staying ahead of regulatory requirements in the biotech and pharma industries means being agile and detail-oriented. Explore our blog to see how Veeva Vault RIM can transform your regulatory processes for greater compliance and efficiency. Discover how to streamline workflows, harness advanced reporting, and optimize your Vault RIM environment for maximum performance. Find out more: https://lnkd.in/e87GXjF4.
Honing Your Vault RIMS Environment for Peak Performance
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#Showcase: Today, AUGUST 7, 2024 - Let's talk about Cloudbyz eTMF with Tunir Kr Das Join us for lunch today at noon (CST) or 1 pm (EST) on Wednesday Live with Cloudbyz, our exciting new weekly demo series. Every Wednesday, we’ll show you how our powerful solutions, like our CTMS, eTMF, and EDC, can streamline your clinical trials. In just 30 minutes, you’ll see real-world use cases and engage in live Q&A sessions with our demo engineering team. About Cloudbyz eTMF: Cloudbyz eTMF solution offers a cloud-based repository of all clinical trial documents including files, images, information, etc. Digitally store, manage, and share all clinical trial-related documents with a centralized overview. Manage essential trial documents, stay inspection ready, and enable real-time visibility for CROs, sponsors, monitors, and other stakeholders in a clinical trial. Reserve your spot now! https://hubs.li/Q02KpM0_0 #CTMS #ETMF #EDC #clinicaltrials #clinicalresearch #pharmaceuticals #medicaldevices #biotech #cloudbyz #salesforce
Wednesday live with Cloudbyz: ETMF | LinkedIn
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Solving IT System Challenges since the 90s!
2moCan't wait to reconnect with everyone - Come by the booth and to learn fme's Veeva capabilities, pick up some swag, and sign up for our prize raffle!