Detailed Technical File Review as per EU MDR 2017/745
Expert Technical File Review
Our team of experienced professionals specializes in conducting thorough and meticulous technical file reviews. We possess in-depth knowledge of the EU MDR requirements and can carefully assess your technical documentation, ensuring it meets the necessary standards. With our expertise, we identify any gaps, inconsistencies, or areas of non-compliance within your technical files and provide you with effective solutions to address them.
Compliance with EU MDR 2017/745
The EU MDR imposes stringent requirements on medical device manufacturers, demanding robust technical documentation to demonstrate compliance with safety, performance, and quality standards. Our technical file review services focus on evaluating key aspects such as design and manufacturing information, risk management documentation, clinical evaluation, post-market surveillance, labeling, and instructions for use. We ensure that your technical files align with the EU MDR requirements and provide you with detailed feedback to achieve compliance.
Tailored Solutions
We understand that each medical device is unique, and the technical documentation must reflect its specific characteristics and intended use. Our technical file review process is tailored to your device and organization, taking into account the specific requirements of your products. We provide customized solutions and recommendations to help you develop and maintain comprehensive technical files that meet the EU MDR standards.
Regulatory Expertise
With extensive experience in the regulatory field, our team possesses in-depth knowledge of the EU MDR and its practical application. We stay up-to-date with the latest regulatory developments and guidelines to ensure our technical file review services are in line with current requirements. By partnering with us, you benefit from our regulatory expertise and gain confidence in the compliance of your technical documentation.
Enhancing Compliance and Market Access
By undergoing our detailed technical file review, you can enhance your compliance with the EU MDR, reduce the risk of non-compliance, and improve your chances of obtaining or maintaining market access within the European Union. Our recommendations and solutions are aimed at helping you demonstrate the safety, performance, and quality of your medical devices to regulatory authorities, notified bodies, and other stakeholders.a
