At QRcompliance, we are dedicated to support QA and RA professionals within the in vitro diagnostic (IVD) medical device sector.

We aim to clarity regulatory requirements and streamline the documentation process. Our commitment to simplifying compliance helps you effortlessly navigate regulatory complexities, ensuring your products adhere to all standards. To further aid this, QRcompliance offers intuitive templates designed for seamless document compliance.

Let QRcompliance be your partner in (IVD) medical device quality and regulatory compliance.

achieve compliance with
Regulation (EU) 2017/746 (IVDR)

achieve compliance with