Continuous publishing streamlines and accelerates the submission process from planning to publishing and fosters a seamless adaptation to industry changes like eCTD 4.0 and IDMP. Learn more https://bit.ly/3RPgewG Regulatory Affairs Professionals Society (RAPS) #regulatoryoperations #submissionpublishing #pharmaceuticals
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Thank you to the Regulatory Affairs Professionals Society (RAPS) for sharing my thoughts on how continuous publishing accelerates the entire submission preparation process and improves submission quality. Smart strategies like this can make companies more flexible, allowing more time for planning and adapting to the changing regulatory landscape, among other things. #regulatoryoperations #submissionpublishing #pharmaceuticals
Continuous publishing streamlines and accelerates the submission process from planning to publishing and fosters a seamless adaptation to industry changes like eCTD 4.0 and IDMP. Learn more https://bit.ly/3RPgewG Regulatory Affairs Professionals Society (RAPS) #regulatoryoperations #submissionpublishing #pharmaceuticals
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In the world of regulatory affairs, everyday counts. But today, we get an extra one! Dive into the regulatory universe with an extra leap. Make the most of this additional time in achieving compliance excellence. Ready to make this leap year count for precision and expertise? Join us on the journey! Visit our website and book a demo now. https://hubs.ly/Q02mFQFH0 #RegulatoryLeapDay #ComplianceMatters #RegulatoryAffairs #Pharmaceuticals #FreyrDigital
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"Founder & Writer of Climatic Change Newsletter | International Speaker | | Bioscientist & Researcher | SZABIST Graduate | Climate Activist Ambassador | Lab Technologist Intern at Dow Hospital |
I recently had the opportunity to attend an insightful webinar on Regulatory Affairs, organized by RxConnectpk. The session was incredibly informative, providing a deep dive into the complexities and latest developments in the regulatory landscape. Thank you to the organizers and speakers for their valuable expertise and practical insights. I’m looking forward to applying these learnings to enhance compliance and streamline regulatory processes in our industry. RxConnect Pk #RegulatoryAffairs #Compliance #Pharmaceuticals #RxConnectpk #ProfessionalDevelopment
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𝐏𝐥𝐚𝐧𝐧𝐢𝐧𝐠 𝐒𝐮𝐛𝐦𝐢𝐬𝐬𝐢𝐨𝐧𝐬 𝐢𝐧 𝐞𝐂𝐓𝐃 4.0: Are you ready to transition to eCTD 4.0 for your submissions? Our recent Regulatory Affairs Professionals Society (RAPS) survey reveals that 67% 𝐨𝐟 𝐫𝐞𝐬𝐩𝐨𝐧𝐝𝐞𝐧𝐭𝐬 are planning to prepare submissions in eCTD v4.0 format. However, some professionals noted that this transition is not within their current scope, they are unsure, or it is not yet required for them. With 𝐨𝐯𝐞𝐫 𝐭𝐰𝐨-𝐭𝐡𝐢𝐫𝐝𝐬 of companies gearing up for #eCTD v4.0 submissions, the question remains: 𝐖𝐢𝐥𝐥 𝐲𝐨𝐮 𝐛𝐞 𝐫𝐞𝐚𝐝𝐲? At Celegence, we offer the skilled, AI-enabled expertise and experience necessary to help #pharmaceutical companies successfully transition to eCTD v4.0. Let’s connect to show you how we can 4𝐱 𝐲𝐨𝐮𝐫 𝐞𝐟𝐟𝐢𝐜𝐢𝐞𝐧𝐜𝐲 𝐠𝐚𝐢𝐧𝐬, and ensure you are fully prepared for this next step in #regulatory submissions. 👉 Gain immediate access to our full #survey results to understand more about the key trends and challenges in regulatory submissions: https://lnkd.in/gFbcm749 #Pharmaceuticals #RegulatoryAffairs #Compliance #eCTD4 #Survey2024 #RegulatorySubmissions #RegulatoryExcellence #LifeSciences
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Ready to break free from paperwork purgatory? Dive into the weekend with our Regulatory Document Management System! Wave goodbye to chaos and sail into streamlined compliance. Enjoy a stress-free weekend, knowing your documents are in expert hands. Here's to smooth sailing and relaxation ahead! #TGIF #RegulatoryAffairs #Pharmaceuticals #DMS #FreyrDigital
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Non-compliance with HA regulations concerning Mutual Recognition Procedure (MRP) are resource intensive for MAH intended to market in concerned European state. A Regulatory partner excelling in GMP, submissions and any follow-up Regulatory activities is essential in such endeavor. Learn more about MRP obligations by clicking here. https://lnkd.in/gp8BabwS #allthingsRegulatory #Regulatoryaffairs #pharmaceuticals #Regulatoryrequirements #productlifecycle #management #partner
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Services Clinreg Partners provide regulatory and clinical research consulting services to companies. Our regulatory and clinical research experts evaluate and provide gap analysis of your current overall state of compliance, and provide a health check road map to ensure requirements are met, and answer any questions that you may have. ClinReg Partners Example of Services: Review and Assess Current State of Your Regulatory Journey and Provide Strategic and Operational Advice & Gap Analysis Analysis of Regulatory Frameworks & Requirements Writing Clinical Protocols & Clinical Evaluations Preparation of Regulatory Submissions such as IND and NDA Preparation of FDA Meeting Requests and Briefing Documents Building Quality Management Systems Development of Target Profile and Labeling Strategy Represent your company to different Regulatory Agencies #regulatoryaffairs #regulatory #regulatorycompliance #pharma #pharmaceutical #pharmaceuticalindustry #pharmaceuticalmanufacturing
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🚀 Looking to Obtain a Drug License? 🚀 Whether you're in the pharmaceutical or healthcare industry, securing the right certifications is crucial for your business. At RegAlliance, we make it easy to apply for and obtain your drug license, ensuring full compliance with regulatory standards. 🔍 Why Choose RegAlliance? ✅ Expertise in Regulatory Affairs ✅ Hassle-Free Licensing Process ✅ Quick and Efficient Support ✅ Trusted by Life Sciences Companies 📞 Contact us today at 7290916993 and take the first step towards seamless compliance! Apply Now and focus on what matters—growing your business! #DrugLicense #PharmaCompliance #RegAlliance #Healthcare #Pharmaceuticals #RegulatoryAffairs #ComplianceExperts #BusinessGrowth
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🌟 Did you know? Over 70% of new active substances launched in the U.S. in 2023 underwent expedited regulatory review. With the push for faster approvals, robust GMP practices are more crucial than ever to safeguard patient safety and product quality. 🔍 Explore the evolving landscape of GMP compliance and the technologies driving change by downloading our white paper. https://bit.ly/4emaYcC #GMP #QualityAssurance #QualityManagement #Pharmaceuticals #MedicalDevices #Compliance #RegulatoryCompliance Vincent F. Cafiso Melissa Noel
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As a regulatory affairs expert, do you often spend time manually updating yourself on global regulatory guidelines? Why not ask Freya instead? - our AI-powered Global Regulatory Intelligence tool Below are examples of everyday pharma regulatory compliance questions you can ask Freya. She'll find the answers and references in seconds, so you can spend your time doing the parts of your job you love the most:) #Pharmaceuticals #RegulatoryAffairs #Regulatorycompliance #RegulatoryIntelligence #FreyrDigital
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