XCMC Consulting

xcmc provides comprehensive executive, operational, audit, qualification, validation, and remediation services to the pharmaceutical, biotech, gene/cell therapy, medical device, and consumer care regulated industries. whether your project is at the very start of a new development, during any and all specific development stages, requiring any sort of validation services for methodologies/processes/manufacturing, conducting routine quality audits, requires any form of fda regulatory services, requires life product life cycle support, is in need of remediation services, needs support for remediation of a 483, warning letter, or consent decree from the fda, we have highly experienced team members that can fully support your immediate needs. by using any and/or all of the services we provide, our team has the fully capability to analyze and support any and/or all parts of your drug product candidate to potentially increase the current fda approval rate of about 14% to as high as almost 5