A Good Foundation: Regulatory Compliance in the Cosmetic Industry
Are you involved with cosmetics and are unsure of your related regulatory requirements? Does hearing about ISO 22716, US FDA 21 CFR Part...
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Training program structure, refine training matrix to configure new learning management systems (LMS) & training support for employees.
Aligned with GAMP 5 methodology, assisted computerized systems validation focused on medical devices, clinical research, pharma & laboratory work.
Evaluation of enterprise resource planning (ERP) and quality management systems (QMS). Internal system appraisal and regulatory assessments.
Ensuring an adequate qualified GXP cloud-based or on-premises applications, infrastructure verification & technology stack control systems.
Develop & implement procedural controls
for establishing proper governance of
your technological assets.