Monroe Medical Device Consulting Announces Key Partnership
August 2013, MMDC provides Regulatory and Quality Assurance expertise, specializing in FDA Class I & II (US) regulatory submissions and compliance. MMDC’s quality objective is to help companies meet the FDA’s QSR and ISO 13485 requirements though the audit process. Additionally, MMDC provides consulting services for developing short and long-term regulatory strategies for new product development, 3rd Party Inspections, and remediation.
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