Digital Template for General Safety and Performance Requirements (GSPR): Designed to Align with the Standards of Regulation (EU) 2017/746 (IVDR) on In Vitro Diagnostic Medical Devices.
This meticulously crafted template provides a simplified approach to the GSPR under the IVDR. This is a pivotal element in maintaining compliance with EU regulations specific to In Vitro Diagnostic (IVD) medical devices.
We offer an intuitive GSPR Checklist Template, customised to accommodate your unique IVD medical devices. This template acts as an invaluable tool in easing the GSPR compliance process, assuring the creation of precise, regulation-compliant documentation with minimal effort.
Price: €45, excl VAT
QRcompliance also offers consulting services to support her customers. We are here to support you through every step of the compliance process.