MIDI

MIDI is an FDA and ISO compliant total product development consulting firm. The medical industry mandates the most detailed and rigorous set of regulatory development requirements, design control procedures and certifications of any product market. MIDI has decades of knowledge and experience within this world. MIDI's DevelopmentDNA process is not... only the company's innovation engine but also the company's formal design control process for the generation of Design Control Documentation, procedure and Design History Files (DHF) for compliance to the FDA Quality System Regulation; section 21 of the Code of Federal Regulations Part 820.30 and International Standards Organization 13485. The company's procedure and process includes documented design inputs, plans, outputs, hazard & mitigation risk analysis, verification & validation, DHF, formal design reviews, and design transfer. The company strives to generate programs that meet stringent quality and regulatory standards while infusing and maintaining innovative design and engineering from project kick-off to completion. This site is protected by copyright and trademark laws under U.S. and International law.Read More