Consulting
Whether you’re faced with remediation resulting from regulatory findings (FDA 483s or Warning Letter) or your objective is to improve quality and compliance before that happens, PathWise can help.
Our experts work in partnership with your organization to deliver products and services that enable a compliant, effective and efficient Quality Management System.
Services and solutions include:
CAPA System Design & Implementation
Current Good Manufacturing Practices (cGMP)
Form 483 and Warning Letter Remediation
Management Control
Through training in PathWise Project Success managers learned a process for the selection and approval of projects. Team leaders and team members acquired the skills to accomplish projects on time and within scope.
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