Struggling with Medical Device Regulations? Get Support from MedTech Quality Experts 💪 Are you overwhelmed by intricate medical device regulations? Having trouble maintaining quality standards or navigating supplier management issues? Don’t let stringent regulatory requirements hold you back from producing innovative medical devices. Get expert support from MedTech Quality Specialists to solve your quality challenges, comply with MDR 2017/745, effectively manage your suppliers, and pass any audit with confidence. We support Medical Device Manufacturers in: Quality Management: ✅ Technical Documentation (MDR 2017/745, FDA, ISO 13485) ✅ Product Development / Design Control ✅ Test Method Validation ✅ Process Validation (IQ, OQ, PQ) ✅ Packaging Validation ✅ Statistics in MedTech ✅ Risk Management Supplier Management: ✅ Supplier Audits ✅ Supplier Development ✅ Sourcing Components (incl. Technical Documentation) Contact us at: office@sifo-medical.com We are happy to answer questions and support you on your quality journey! ---------------------------------------------------------------------------------------------------------------------- 🌐 If you want to learn more about SIFo Medical, check out our website where you will find valuable resources, like blog posts, checklists, or templates: https://www.sifo-medical.com/ Don't forget to subscribe to our SIFo Medical YouTube channel to receive more valuable expertise about Quality- and Supplier Management in Medical Device Manufacturing. 📩 If you want to be the first to receive updates on blog posts, video content, and valuable insights in MedTech, subscribe to our newsletter: https://www.sifo-medical.com/newsletter #medtech #medicaldevices #medizintechnik #regulatoryaffairs #medicaldevicemanufacturing #qualitycontrol #qualityassurance #medicaltechnology #testmethod #validation ---------------------------------------------------------------------------------------------------------------------- At SIFo Medical, we are passionate about empowering MedTech companies in Quality- and Supplier Management. From our base in the Austrian Alps, we provide MedTech manufacturers with our expertise in Quality Management, especially with: - Compliant Technical Documentation - Internal & External Audits - Test Method Validation - Product Development - Process Optimization - Packaging Validation - Process Validation - Risk Management - Design Control - Statistics On YouTube, our experts provide short, informative, and easy-to-digest videos about medical device Quality- and Supplier Management to support MedTech manufacturers to produce safe medical devices and comply with necessary regulations and standards (like ISO 13485, MDR 2017/745 or FDA requirements). Expand your knowledge in MedTech and profit from 10.000+ hours of practical expertise in the medical device industry. Subscribe to SIFo Medical today and never miss out on valuable MedTech expertise. Follow us: YouTube: @SIFoMedical LinkedIn SIFo Medical: https://www.linkedin.com/company/sifo... LinkedIn CEO Simon Föger: https://www.linkedin.com/in/simonfoeger/ TMV Online Guides: www.testmethodvalidation.com Website: www.sifo-medical.com Newsletter: https://www.sifo-medical.com/newsletter Related Topics: Medical Device Consulting Quality Management Supplier Management Process Validation Operational Qualification Installation Qualification Performance Qualification Test Method Validation