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...
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.