Medvacon is a leading provider of quality compliance and validation services in the life sciences industry, specializing in FDA 483 warning letter remediation, inspection readiness, and quality system audits. They also offer regulatory compliance consulting, laboratory services, and training in cGMP compliance and project management.
With a certified minority business enterprise (MBE) and small business enterprise (SBE) status, Medvacon is committed to delivering high-quality services to their clients. Their experienced leadership team and comprehensive range of services make them a trusted partner for companies in need of quality compliance and validation solutions.
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