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January 30, 2026 at 4:32 AM
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January 21, 2026 at 3:30 AM
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January 16, 2026 at 5:10 AM
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January 12, 2026 at 10:22 AM
eCTD is evolving—and eCTD v4.0 is the future.
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January 7, 2026 at 11:50 AM
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Regulatory Document Publishing is no longer optional—it’s mission-critical. 🚀
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January 5, 2026 at 9:22 AM
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December 8, 2025 at 10:18 AM
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Dual Specialization: Drug Regulatory Affairs + Pharmacovigilance
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November 27, 2025 at 5:45 PM
Dual Specialization: Drug Regulatory Affairs + Pharmacovigilance
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✨ #RWD & #RWE
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Now updated with:
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🌍 Global Medical Device Regulatory Affairs Course with AI — Future-Ready for 2026!
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November 24, 2025 at 7:33 AM
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November 20, 2025 at 4:05 AM
🚀 The future of #RegulatoryAffairs is AI-enabled!
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🚀 EPGiDRA: Executive Program in Global & AI-Driven Drug Regulatory Affairs
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November 18, 2025 at 6:50 AM
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💡 Biopharma is where science meets strategy — the epicenter of innovation, investment & global growth.Master how R&D, business & commercialization come together in biologic business. 🌍
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How to Master Biopharma Business?
Learn how to master biopharma business and navigate drug discovery and development for a successful career in the industry.
royed.in
November 12, 2025 at 7:16 AM
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EPLsRA by Royed Training blends AI-powered submission management, eCTD v4.0, & CMC authoring for cross-domain mastery — Pharma, Biologic, Device, Food & more.
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November 10, 2025 at 3:49 AM
EPLsRA by Royed Training blends AI-powered submission management, eCTD v4.0, & CMC authoring for cross-domain mastery — Pharma, Biologic, Device, Food & more.
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Upskilling in ASEAN Drug Regulatory Affairs: Building Regional Expertise for a Stronger Pharmaceutical Future
Become an expert in ASEAN Drug Regulatory Affairs. Our course covers country-specific regulations and practical solutions.
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November 9, 2025 at 11:31 AM
🌸 Master the science behind cosmetic Regulation!
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November 8, 2025 at 5:30 AM
🌸 Master the science behind cosmetic Regulation!
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🚀 Master the Biopharma Business—from R&D to Global Market!
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November 3, 2025 at 5:07 AM
🚀 Master the Biopharma Business—from R&D to Global Market!
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💡 Turn real-world data into real impact!
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November 1, 2025 at 7:01 AM
💡 Turn real-world data into real impact!
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💼 Master business expansion, licensing, tendering & market access strategies tailored for the Middle East region with Royed Training’s Pharma Business Development Certification.
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October 31, 2025 at 3:32 AM
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What is RAID Designation by the SFDA?
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What is RAID Designation by the SFDA?
What is RAID designation? Understand its significance for investigational drugs and the R&D landscape in Saudi Arabia.
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October 30, 2025 at 8:55 AM
What is RAID Designation by the SFDA?
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🌍 Step into Global Regulatory Affairs! 🤖✨
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💡 Includes AI in Regulatory Affairs module!
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October 25, 2025 at 2:30 AM
🌍 Step into Global Regulatory Affairs! 🤖✨
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🌎 Learn Pharma Business Development in LATAM!
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October 22, 2025 at 6:43 AM
🌎 Learn Pharma Business Development in LATAM!
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💼 Step into the world of Life Science Consulting!
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October 22, 2025 at 4:16 AM
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🎆 Happy Diwali from Royed Training! 🎇
May this Festival of Lights bring you success, knowledge, and endless opportunities to shine brighter in your professional journey. 🌟
✨ Keep learning. Keep growing. Keep glowing.
— Team Royed Training 💫
#royedtraining #royedin
May this Festival of Lights bring you success, knowledge, and endless opportunities to shine brighter in your professional journey. 🌟
✨ Keep learning. Keep growing. Keep glowing.
— Team Royed Training 💫
#royedtraining #royedin
October 20, 2025 at 5:16 AM
🎆 Happy Diwali from Royed Training! 🎇
May this Festival of Lights bring you success, knowledge, and endless opportunities to shine brighter in your professional journey. 🌟
✨ Keep learning. Keep growing. Keep glowing.
— Team Royed Training 💫
#royedtraining #royedin
May this Festival of Lights bring you success, knowledge, and endless opportunities to shine brighter in your professional journey. 🌟
✨ Keep learning. Keep growing. Keep glowing.
— Team Royed Training 💫
#royedtraining #royedin
🚀 Master the future of CMC Documentation & AI in Regulatory Affairs 📑🤖🌍
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September 29, 2025 at 2:30 AM
🚀 Master the future of CMC Documentation & AI in Regulatory Affairs 📑🤖🌍
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