The 4th Annual Pharmaceutical Regulatory Affairs Summit is almost over, and we want to take a moment to express our deepest gratitude to all the speakers, participants, and sponsors. We value your support, your contributions, your feedback, and we thrive on becoming better and better with each hosted conference. We genuinely hope that the summit has left you with only positive impressions and loads of information to process and find ways to make them become real. Let’s continue to work together on a bright and innovative future! #summit #event #pharmaceutical #pharma #regulatoryaffairs #vienna #trends #pharmaregulatorysummit #industryexperts #regulatoryaffairs #pharmaceuticaltrends #thankyou
Allan Lloyds’ Post
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In our series of regulatory approvals across different countries, we present our latest whitepaper focused on the approvals by the Swissmedic. #swissmedic #regulatory #drugapprovals #indicationextension #pharma
📣 Explore the latest regulatory developments in the pharmaceutical industry! Our white paper 📄 delves into Swissmedic's recent authorization of 41 human medicinal products with new active substances, providing valuable insights into the evolving landscape of drug approvals. Stay informed and gain a deeper understanding of regulatory trends by accessing our white paper today, For more informative updates, visit 🌐 www.vyuhpharma.com #PharmaRegulations #RegulatoryTrends #WhitePaper #PharmaceuticalIndustry #pharmanews #pharmaceutical #healthcare #pharmaceuticalindustry #Swissmedic #PharmaceuticalRegulation #DrugApprovals #Healthcare #PharmaIndustry
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Aspiring Pharmaceutical Technologist || B.Pharm || Six Sigma White Belt || CRM ||Good Clinical Practices(GCP) || Campus Ambassadors || Aspire Leader by Harvard Business School || AI || Digital marketing ||
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🆕 We are very pleased to announce that Paul Attridge from Veeva Systems will speak during our upcoming live webinar. The webinar will provide you with useful information to better manage IDMP-related activity to comply with regulatory requirements. As insights from the pharmaceutical industry, Daniele Segagni from MENARINI Group will talk about the company's experience and the impact of IDMP. An interesting opportunity to explore the topic and solve your doubts! 🔔 Reserve your seat now (limited seats) 👉 https://lnkd.in/dJMQv-vQ #IDMP #EMA #pharmaceutical #regulatory #drugsafety #lifescience #webinar
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The year 2023 and early 2024 witnessed a host of significant #pharmaceutical regulatory reforms, with the most extensive overhauls occurring in #APAC's largest markets. These reforms are reshaping the regulatory framework and commercial dynamics for international pharmaceutical enterprises operating in these territories. Read on to discover the opportunities and challenges present in the APAC #medicine sector: https://lnkd.in/ecNbKkMW #ConnectedThinking
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#1 Best Selling Author • Inventor of Qi Coil™ • Health and Wellness Entrepreneur • Executive Producer • Martial Artist
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Have you already reserved your place for our upcoming live webinar? The webinar will provide you with useful information to better manage IDMP-related activity to comply with regulatory requirements. As insights from the pharmaceutical industry, we are very pleased to welcome Daniele Segagni from MENARINI Group: he will talk about the company's experience and the impact of IDMP. An interesting opportunity to explore the topic and resolve your doubts. Reserve your place now (limited seats) 👉 https://lnkd.in/dJMQv-vQ #IDMP #EMA #pharmaceutical #regulatory #drugsafety #lifescience #webinar
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REAL RESULTS: TRANSFORMING COMPLIANCE CHALLENGES INTO SOLUTIONS Collaboration and expertise shine brightest when faced with real-world challenges, as evidenced by the testimonial from the Head of Global Compliance at a leading pharmaceutical company. At Quality Executive Partners (QxP), our focus is on delivering straightforward solutions, enabling organizations to maneuver through regulatory complexities with clarity and assurance. Connect with us today to learn how QxP can guide your path to regulatory excellence. 👉 https://lnkd.in/ezQG6u6B #pharmaceuticals #pharma #biotech #qualityassurance
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Was this a good year for pharma? Were approvals more or less compared to 2022? How many inspections were conducted and how many warning letters were issued? Download a concise summary from our regulatory and manufacturing team here - https://lnkd.in/eavpn4Zk #FDAInsights #PharmaRegulations #RegulatoryTrends #WhitePaper #pharmaceutical #CDER #FDA
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