Guarantee the safety and quality of all your medical devices. Cover all aspects of your medical devices, from design and development to post-market surveillance and labeling requirements, with an EU MDR audit checklist app.
Easily comply with the EU MDR regulations through digital checklists. Cover all aspects of the regulations from design and development to safety and quality of the manufactured medical devices and tools.
Maintain all records and documents to support your claims about the safety and efficacy of your devices. Streamline data imports and exports between different platforms. Gather all the critical data in centralized cloud storage.
Guarantee the safety and performance of your medical devices. Auditors can quickly notify the problems in the design, packaging, manufacturing, or functionality and get them fixed before it reaches Europe for sale.
Quickly access all the data at your fingertips. View the performance of all your medical equipment. Look closely at all the information and gather insights. Keep track of all the audit results to see which devices require improvements.
Thanks to the cloud-based no-code architecture, you don’t need to worry about updating or upgrading your applications. Continue your work with productivity without any delays in app up-gradation or worrying about new rules and compliance.
Axonator provides purpose-built enterprise solutions configured to each customer’s specific needs. Contact us now to learn how Axonator can work for you.
Axonator is a no-code, mobile-first field workflow automation platform that helps organizations automate and optimize their field performance, improve customer service, and scale operations.
