Inside Interius' Global Regulatory Strategy https://lnkd.in/exM8gQn6 - By Matthew Pillar, Editor, Bioprocess Online As the trend toward seeking efficient and expeditious clinical progress goes, Interius has orchestrated a global regulatory strategy that’s centered in Australia.
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The recommendation of improving stakeholder interaction is a common conclusion of our Expert Meetings in a broad range of regulatory topics. This is also reflected in the two recently published articles based on Regulatory Science Network Netherlands Expert Meetings in Drug Discovery Today. The first one focuses on the discussions and findings from the RSNN Expert Meeting "Regulator-initiated studies for regulatory decision making": https://lnkd.in/dNJe3Ggs The second one highlights the discussed topics and recommendations from the RSNN Expert Meeting "Addressing the framework of unmet medical need": https://lnkd.in/dZdfAsxn Both articles are also available on our news & events page of our website linked below. #multistakeholder #regulatoryinnovation #articles
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Curious about how to successfully navigate complex global regulatory landscapes and ensure market access? Join us for an informative webinar packed with expert insights and strategies—don’t miss out! Meriem Gaval Cruz, PhD, RAC (Drugs) #regulatorystrategy #regulatoryintelligence #drugdevelopment
Join us for November's Complimentary session of Vivpro Corp's Regulatory Briefs | Webinar Series! We will gain insights on 𝐆𝐥𝐨𝐛𝐚𝐥 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐒𝐭𝐫𝐚𝐭𝐞𝐠𝐲 from Dr. Meriem Gaval Cruz, Director, Global Regulatory Lead at Novo Nordisk. 🗓 Date: Wednesday, November 20th ⏰ Time: 11:00 AM ET Wondering how to harmonize your global registration strategy while meeting each market's unique needs? Want to learn strategies and insights from an expert? Join our webinar to find out more! 🎟 Register here: https://lnkd.in/eSCBX5xq 💬 Check out what previous attendees are raving about: "𝐄𝐱𝐜𝐞𝐥𝐥𝐞𝐧𝐭 𝐢𝐧𝐬𝐢𝐠𝐡𝐭𝐬 𝐚𝐧𝐝 𝐩𝐫𝐚𝐜𝐭𝐢𝐜𝐚𝐥 𝐞𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞𝐬." 🔄 We invite you to explore our previous sessions by visiting our YouTube Channel ➡ https://lnkd.in/enrHQdsg
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Regulatory Affairs Professionals Society (RAPS) recently published an article concerning the usefulness of real-world evidence (#RWE) for #medicaldevices. Current barriers and solutions are discussed as well as the need to adopt RWE focused regulatory policies. https://lnkd.in/gdqxAj66
Expediting regulatory guidance for RWE in medical devices: Why it matters for patients
raps.org
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Working with a clinical research partner who understands regulatory requirements at a global level, combined with country-specific knowledge, will provide you with many benefits. Advanced Clinical can help define global and/or local regulatory strategy and successfully deliver a project, no matter the size or the type of product. Learn more how we can support your regulatory needs: https://hubs.la/Q02M702s0 #RegulatoryAffairs #ClinicalResearch
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Chief Product Officer | MedTech Consultant and Advisor | Fractional CPO | CMO | SVP | Strategy and Product Management Executive
If you operate in life sciences this is important because... "Emerging RWE-focused regulatory policies and guidance are supporting this momentum, helping to codify best practices and provide stakeholders with guidance on expectations for "regulatory-grade" RWE generation." Quality Means Business https://lnkd.in/guCH_sKh
Expediting regulatory guidance for RWE in medical devices: Why it matters for patients
raps.org
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New Blog: Trinity ReguMed Insight: Revolutionizing Regulatory Management for the Life Sciences Industry. Read more below. https://wix.to/xUxBWnI #trinityregumed #trinitymconsulting #RIM #newblogpost
Trinity ReguMed Insight: Revolutionizing Regulatory Management for the Life Sciences Industry
trinityregumed.com
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Ready for the final day of RAPS US Conference 2024? We sure are! 🚀 If you're looking for expert guidance on regulatory affairs in life sciences, stop by booth 539 to connect with our team. Antonio, Pieter, and Jens are eager to share insights and help tackle your regulatory challenges. See you there! 👋 #RAPSConvergence #LifeSciences #RegulatoryAffairs
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Advisory Committees Give FDA Critical Advice and the Public a Voice At the FDA, we rely on our many advisory committees to help us make sound decisions based on the best science available. Advisory committees give our own FDA experts outside, independent, and professional advice on various complex scientific, techni... https://lnkd.in/dzV8pnmT #BioTech #science
Advisory Committees Give FDA Critical Advice and the Public a Voice
openexo.com
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Did you miss the live webinar on Current Clinical #Pharmacogenomic (PGx) Testing? The presentation recording is now available online. Dr. Yuan Ji covers the latest in technologies, guidelines, and regulatory frameworks driving clinical PGx testing. https://ow.ly/oyn550SNynP
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Adapting to Regulatory Changes: A Key to Innovation At Notable Labs, we prioritize staying ahead of regulatory updates to maintain compliance and drive scientific progress. Engaging with regulatory bodies and industry forums helps us navigate changes smoothly, ensuring the highest standards in our research. #NotableLabs #RegulatoryCompliance #BiomedicalInnovation
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