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As an IVD manufacturer, you must ensure that your product meets the relevant regulatory requirements before being placed to the market.
It is critical to work with a trusted EU Notified Body or UK Approved Body that understands the industry and has the experience to review and confirm your product’s readiness for market.
We truly understand the challenges that medical devices manufacturers face bringing compliant products on to market efficiently and safely. Whether you're starting the certification process or looking to transfer to BSI, we offer a range of flexible product review services providing you with efficient pathways to bring your product to market.
As a manufacturer of IVD medical devices, one of your biggest challenges in breaking into, or continuing your success in, this market is navigating the regulatory process efficiently. Strong, statistically relevant clinical data demonstrating the safety and performance of your device is essential to ensuring a successful outcome of your IVDR application.
Our IVD team has a broad range of industry and regulatory experience, including product design and development, manufacturing, testing and regulatory expertise. They will support you through the process of certifying your device.
Download our IVD brochure to learn more about how we can support your product launch.
Nous proposons des formations adaptées au règlement sur le diagnostic in vitro pour vous aider à soutenir et à développer votre activité.
