QAEC Limited - Quality & Regulatory Consulting Services |Life Sciences |Manufacturing reposted this
⏳ With just weeks to go until the critical 26th September 2024 deadline for the EU MDR 2017/745, the clock is ticking for legal manufacturers of legacy devices. Are you confident that your organization is fully prepared to leverage the extension provisions under EU 2023/607? This extension offers a vital opportunity for manufacturers to stay compliant, but the time to act is NOW. If you haven’t already ensured that your legacy devices are in line with the necessary requirements, now is the moment to reassess your compliance strategy and avoid potential disruptions. 💡 Is your organization ready? If not, partner with QAEC Limited to help you through a seamless transition. Here’s how we can help: ✅ Compliance Strategy: We assess your current status and develop a clear roadmap to meet MDR requirements. ✅ Documentation Support: From clinical evaluations to technical files, we help prepare and review key documentation. ✅ Regulatory Expertise: Navigating the complexities of EU 2023/607? We provide expert guidance on the extension provisions. ✅ Risk Management: We identify and mitigate compliance risks, ensuring that your products remain on the market. With the clock ticking, now is the time to ensure your legacy devices are future-proofed. QAEC Limited consultancy services are tailored to meet your needs at competitive and cost-effective rates. Contact me today at charles.spearpoint@qaeclimited.co.uk. #EUMDR #MedicalDevices #RegulatoryCompliance #MedicalDeviceRegulation #EU2023607 #HealthcareCompliance #QAECLimited