“RamSoft is committed to innovating while maintaining the effectiveness of our Quality Management System based on ISO 13485, allowing us to deliver software and services that exceed the expectations of healthcare professionals and enabling better patient care”
— Vijay Ramanathan, President & CEO
Quality Management System
Our QMS is regularly audited by a registrar –SGS– to certify our compliance to MDSAP ISO 13485:2016 requirements including Canadian regulations, and FDA’s Quality System Requirements. RamSoft’s quality management system also complies with the European Union Medical Device Directive.
Quality Assurance Policy Principles
Executive Management will ensure that the Quality Policy is appropriate to the purpose of the Company, and includes a commitment to comply with the requirements of both customers and regulatory authorities and continually improve the effectiveness of the Quality Management System. The Quality Policy will provide a framework for establishing and reviewing the policy for adequacy and suitability on a regular basis while ensuring that the Quality Policy is communicated and understood within the Company.
It is important to note that the above quality policy discusses maintaining the Quality Management System. The use of the word maintaining is taken to mean not only the maintenance of the existing system but ensuring that the system is maintained in accordance with the requirements of applicable regulatory authorities. This policy ensures that RamSoft’s Quality Management System meets not only the requirements of our users but also all legal requirements in the countries where RamSoft conducts business.
Resources & Conformance Statements
We take standards compliance very seriously here at RamSoft. That’s why we follow strict quality assurance protocols when developing our products to exchange, integrate, share, and retrieve patient data from 3rd party vendors. See below for our conformance statements and resources.