While this marks the end of a product’s market journey, the manufacturer’s responsibilities don’t simply vanish.
📋 Even after distribution has ceased, manufacturers must retain technical documentation for a specified period—depending on the device’s risk category.
🔍 Responsible manufacturers continue monitoring devices that remain in use, ensuring patient safety and regulatory compliance.
At BiTrial, we provide comprehensive support throughout the entire lifecycle of medical devices, from development to post-market activities and beyond. 🚀
🤝 Contact us and let’s see how we can assist with your medical device development!