We perform state-of-the-art medical device security design, architecture review, product security testing, assessments and validation of security design and requirement implementation. Security testing and requirement analysis performed via globally accepted product security verification practices through code review, application security testing, security threat process development and improvement, fuzzing, run-time testing and secondary attacks. Expert analysis performed in accordance with global product security regulations. (ISO 60601, ISO 13485, FDA pre and post market security guidance).