Cosmetic GMP: ISO 22716 Implementation
Translate cosmetic GMP principles into usable production controls, records and staff responsibilities, with practical examples for your manufacturing operation.
Private group · Scope-based quotation · Live online · On-site by arrangement
Indicative syllabus
- Personnel, premises, equipment and hygiene
- Raw materials, packaging materials and production controls
- Quality control, finished-product release and storage
- Documentation, change control and deviations
- Subcontracting, complaints, recalls and internal audits
- Process-based exercises and an agreed assessment
What the certificate means
An FDABridge certificate records completion of the agreed course and its participation or assessment requirements. It is not FDA approval, personnel certification or certification of your organization.
Training is separate from regulatory filings, consulting, remediation and certification. The final scope and price are stated in the written proposal.
Learning outcomes
- Map the main ISO 22716 GMP controls to your operation.
- Recognize evidence needed for production, release, hygiene and traceability.
- Prioritize gaps and plan practical implementation steps.
Who it is for
Cosmetic manufacturers, quality and production managers, supervisors and internal-audit teams.
What we need to tailor it
- Manufacturing activities, product types and site count
- Existing GMP arrangements and the team's learning priorities
- Participant roles, experience and group size
- Preferred format, language and training period
Scope boundaries
- This course does not certify the facility to ISO 22716.
- Site auditing, implementation consultancy and writing a complete SOP system are separately scoped.
- ISO 22716 training does not by itself establish compliance with every applicable U.S. cosmetic requirement.
What your written proposal confirms
Training is separate from regulatory filings, consulting, remediation and certification. The final scope and price are stated in the written proposal.
An FDABridge certificate records completion of the agreed course and its participation or assessment requirements. It is not FDA approval, personnel certification or certification of your organization.