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Equip your business for regulatory approvals with Pi Pharma Intelligence. Our insights help you understand the landscape and identify potential hurdles. Book your FREE demo today by heading to https://lnkd.in/gZzaMVWA #pharmaintelligence #Regulatorydata

Bringing a new drug to market is no small feat, and navigating the clinical trial process can be daunting. DocXellent's Pharma Regulations 101 dives deep into the key regulations governing the pharma industry, empowering you to make informed decisions every step of the way. Read more here: https://hubs.li/Q02lkjpV0 #clinicaltrials #DocXellent

Watch our TOPRA - The Organisation for Professionals in Regulatory Affairs sponsored webinar: Integrated Pharma Regulatory Strategy as the Key to Market Advantage. Are you struggling with a fragmented regulatory approach that’s slowing down your innovative therapies? This webinar will equip you with the power of an Integrated Pharma Regulatory Strategy. Our experts will reveal how to: * Unify your regulatory efforts for a streamlined path to market. * Minimize risks and navigate complex frameworks with confidence. * Shave valuable time off your development timeline. Click here for the full recording and access to the slides. https://lnkd.in/eJ8_frHF Kate Coleman Jayne Hunt Sam Tomlinson Sandra Lourenço Erik Smit #pharma #regulatory #quality

Integrated Pharma Regulatory Strategy as the Key to Market Advantage. Are you struggling with a fragmented regulatory approach that’s slowing down your innovative therapies? This webinar recording from Arriello and TOPRA reveals how to: * Unify your regulatory efforts for a streamlined path to market. * Minimize risks and navigate complex frameworks with confidence. * Shave valuable time off your development timeline. Click here for the full recording and access to the slides. https://lnkd.in/eJ8_frHF #pharma #regulatory #quality

Do you feel overwhelmed when it comes to your drug submission? Let me help you delve into all the complexities. 🚀 Take part in the latest 𝗦𝗖𝗛𝗢𝗧𝗧 𝗣𝗵𝗮𝗿𝗺𝗮𝘃𝗲𝗿𝘀𝗶𝘁𝘆® session and gain insights on streamlining your testing processes for regulatory compliance, accelerating your market submission, and elevating the assurance of your product’s quality and safety. Let's talk about considerations of electing a container in Early Clinical vs. Preparing Container Drug Submission. Why is building and maintaining solid expertise in testing activities for internal teams often difficult? How to turn the root cause into a solution? And how important are mistakes? I look forward to my webinar, What to test and what not to test, that is the question for your drug submission, on March 13th, 2024 | at 4:00 PM (CET). 👉 Sign up here: https://lnkd.in/dsTSps6A #pharmaversity #SCHOTTPharma #pharma

When it comes to start-up biotech, pharma and life sciences companies, being small doesn't exempt you from complying with FDA regulations. Check out our latest blog post to learn why, and what you need to do to prepare for a successful #eCTD submission. https://lnkd.in/g6h_Hghb #regulatorycompliance #fdasubmissions #fdaregulations

LOUD REMINDER for DocuSign live webinar in 5days time. Learn more about the regulatory compliance for contract management in India's Life Sciences and Healthcare industry.