Acquisition Assessment and Remediation
The Risk Assessment was leveraged to assure the testing methods were effective as well as efficient.
The RND Group leveraged the client’s quality management system allowing for a seamless handover at the end of the project. All user needs, requirements and verification test cases were written and managed in JAMA allowing for efficient collaboration with a distributed team (Chicago, Indianapolis, Dallas and Milan Italy).
The project demonstrated that an existing product can be brought into line with the FDA documentation requirements. The RND Group’s extensive knowledge of medical device standards allowed us to assess the gaps, develop a plan to address the deficiencies and execute the plan to bring the product into compliance.
With over 20 years of experience in regulated software engineering, we’ve built a heritage and reputation for building specialized software with precision and care. The RND Group can point with pride to products that have been successfully introduced into the medical device marketplace.
Software Technologies
Capabilities Applied
Microsoft Windows 2012 Server – Target OS
JAMA – Requirement, Test Case & Test Execution
Oracle 11.2 – Target Database
LIS2-A2 / ASTM 1394 – Laboratory Communications
Oracle Virtual Box – Test Environments
FDA Part 820, Part 11
Requirements development and management
ISO 13485, HIPAA, IEC 62304
Software risk analysis and management
Software life cycle processes
Project management
Software verification