# Precision Digital Health — May to August 2026

# Precision Digital Health — May to August 2026

Edward led software quality assurance and compliance enablement for clinical-trial SaaS built to medical-device standards: ISO 13485, IEC 62304, and ISO 14971, in an FDA audit context.

He reconstructed a formal requirements baseline and traceability for a platform delivered without supporting documentation. He built and demonstrated an AI-driven automated regression tool operating inside the regulated software lifecycle and established the JIRA evidence structure adopted as the company's ongoing quality standard.