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CaliberQAMS offers you a highly configurable, workflow-driven process automation designed as per 21CFR Part 11and cGMP regulations. CaliberQAMS helps you in Creation, Review, and Approval of change request, deviation recording, and hence, automating your entire QA process. This results in easy planning, scheduling and executing self-inspections , vendor audits, and regulatory audits. Through an integrated approach, CaliberQAMS facilitates task management of follow-up actions through CAPA and Training.