Roundtable Discussion: Bridging the Gap Between Agile Methodology’s Iterative Nature with the Strict Documentation & Validation Required by Regulatory Bodies to Ensure Ongoing Compliance - 3rd Medical Device Software Development Europe

Roundtable Discussion: Bridging the Gap Between Agile Methodology’s Iterative Nature with the Strict Documentation & Validation Required by Regulatory Bodies to Ensure Ongoing Compliance

Time: 12:00 pm
day: Conference Day Two

Details:

Integrate rigorous documentation processes within agile sprints to maintain regulatory compliance while preserving flexibility
Schedule regular compliance checkpoints to ensure that iterative changes align with regulatory requirements and validate each increment
Utilize automated tools to track changes and maintain comprehensive records, ensuring traceability and adherence to regulatory standards throughout development