ACSYS, Inc. specializes in developing world-class Quality and Compliance capabilities. Their associates offer extensive knowledge and best practices to deliver effective recommendations for improvement in Clinical Research, Quality Systems, and Design Controls Process Excellence. ACSYS focuses on FDA and European Medical Device Directive Readiness, Manufacturing Process/Systems Transfer, Validation, Regulatory Submissions, Audits, and Product Development. They assist clients in enhancing regulatory compliance, increasing speed to market, improving product quality, and optimizing product and process development through the implementation of high-performing systems.