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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

#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.

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

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.

Unlock the full potential of Veeva Vault RIM! Discover tips to optimize regulatory processes and ensure efficiency in our blog.

Streamline regulatory compliance with Veeva Vault RIM! Learn how to enhance workflows and optimize performance in our blog.

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!

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.

Streamline regulatory compliance with Veeva Vault RIM! Learn how to enhance workflows and optimize performance in our blog.

#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