EXTEDO’s Post

🎤There's just 2 more weeks to go until RESCO Europe!!🎤 CLIN-r+ are delighted to announce their participation at the RESCON EUROPE 2024 supporting planning of sustainable MedTech. Our Director of Clinical and Regulatory Affairs, Jacqueline van Druten will be supporting the Sustainability discussions on Respiratory MedTech: ☀️Day 1 – Session 3 Sustainable Development and Environmental Impact ☀️ 1️⃣12:30 – 13:00 The Innovation Imperative: Regulatory & Design Strategies for a Sustainable Competitive Advantage in Respiratory Devices 2️⃣16:00 Panel discussion: Charting the Future of Inhalation Therapies: Innovations, Regulations, and Market Trends We hope you can join us!! We always enjoy a catch-up and chat, and you are also welcome to make an appointment with us in advance to discuss your regulatory or clinical affairs needs to obtain your MDR CE mark or your GREEN transition. During the event, we will be offering clients a free 40-minute consultation (at the event or virtually) to discuss your most pressing EU MDR Clinical Regulatory questions. 💥BOOK YOURS NOW: https://loom.ly/bnNk7co 💥 ➕Download the RESCON Europe 2024 Official Brochure here: https://loom.ly/D3YywlE #RESCON2024 #RESCONEUROPE #medtech #sustainability #regulatoryaffairs

When LinkBio Corp. needed a powerful solution for post-market surveillance, they turned to PatientIQ. By leveraging our ResearchPRO platform, they streamlined their processes, achieved meaningful results, and unlocked $5 million in new revenue within just 60 days—all while staying ahead in regulatory compliance and data collection. Discover how PatientIQ supported LinkBio Corp. in improving efficiency and driving measurable outcomes. 📖 Read the full story here: https://hubs.la/Q02_8FPV0

📣 NEW SOLUTION. SERO AS - The independent control sera specialist, a Norwegian pioneer in quality control materials, is setting new standards for reliable laboratory testing. With their innovative Seronorm® products, they're ensuring that doctors and patients can trust their lab results. 🧪 In a world where accurate diagnoses are crucial, SERO is leading the charge. Curious to know more? Read the full article here: https://ow.ly/Swix50TaufI #HealthTech #LabTesting

Our latest #FDARegulatoryNewsandTrends

Meet us @RAPS and join our discussion how #startups can benefit in #supplychain and #procurement leveraging a solid regulatory strategy.

One of today’s sessions at #TOPRASYM24 focused on the complexity of clinical trial innovation across borders and the evolution of regulatory infrastructure in Europe as alignment initiatives continue. The bottom line: it takes time to do it right—and honest conversations between regulatory authorities and companies to put patients first. The good news: trust is being built and progress is happening through transparent stakeholder collaborations. Well done, Maren Koban, Susan Bhatti, Lada Leyens, Katarina Nedog, Kit Roes, Begoña Nafría Escalera and Ana Zanoletty.

🔔 New upcoming MedBoard Webinar 🔔 How to build an effective Regulatory Intelligence System + Live Demo, MedBoard Step by Step 📌 Join us on December 12th at 16:00 UTC 👉 Registration link in the comments 👈 In this Webinar, we will explore how Regulatory Professionals can master and build an effective Regulatory Intelligence process within the organizations while facing the current extraordinary increase in data, news, requirements, and information shared from different sources. Ivan Perez Chamorro will share knowledge and experience gained through at MedBoard, where we support thousands of Regulatory Professionals in efficiently keeping compliance with more than 15 regulatory areas! ▶️ See you there! #medboard #webinar #regulatoryintelligence #rims #impactassessment #regulatory #compliancemonitoring #countriesregistrations #productsinformation

Peyton Howell joined other industry leaders at DPHARM to discuss innovative solutions to major challenges in clinical trials. Key topics included 🔹 how organizations are adapting by optimizing resources and embracing innovation 🔹 the focus on automation, technology and patient-centricity 🔹 regulatory changes requiring proactive engagement 🔹 upfront investments needed for improvements. Check out this recap of the panel in Applied Clinical Trials Magazine: #Dpharm2024 #DiscruptiveInnovations

IDMP is changing the way regulators, manufacturers, healthcare providers, and wider stakeholders exchange information about medicinal products worldwide. But implementing this game-changing initiative is no small feat. Our guide will help you prepare and give you some helpful tips and tricks for success. Download it here : https://lnkd.in/efktPPbm #IDMP #lifesciences #regulatoryaffairs #datamanagment

Peyton Howell joined other industry leaders at DPHARM to discuss innovative solutions to major challenges in clinical trials. Key topics included 🔹 how organizations are adapting by optimizing resources and embracing innovation 🔹 the focus on automation, technology and patient-centricity 🔹 regulatory changes requiring proactive engagement 🔹 upfront investments needed for improvements. Check out this recap of the panel in Applied Clinical Trials Magazine: #Dpharm2024 #DiscruptiveInnovations