
Master ISO 22716 Good Manufacturing Practices to strengthen cosmetic product quality, safety, compliance, and manufacturing control.
Created by SF Trainings Team
The ISO 22716 GMP: Best Practices for Cosmetic Manufacturing course provides practical knowledge of Good Manufacturing Practices specifically applicable to the cosmetics industry.
It covers key ISO 22716 requirements related to personnel, premises, equipment, materials, production, quality control, documentation, complaints, recalls, deviations, subcontracting, and internal audits.
Participants will learn how to establish controlled manufacturing processes that support product quality, consumer safety, traceability, and regulatory compliance.
The course also explains how to manage non-conforming products, waste, lifecycle risks, change control, and inspection-ready documentation effectively.
By completing this course, learners will be better prepared to implement, maintain, monitor, and continually improve GMP practices within cosmetic manufacturing operations.
You will learn to:
ISO 22716 Fundamentals
Understand the purpose, scope, structure, and core principles of Good Manufacturing Practices for cosmetic products.
Personnel & Hygiene
Learn how personnel competence, responsibilities, training, health, and hygiene support effective GMP compliance.
Premises & Facilities
Understand how facility design, layout, cleanliness, and environmental controls help prevent contamination and product mix-ups.
Equipment Management
Learn requirements for suitable equipment, qualification, maintenance, calibration, cleaning, and controlled use.
Raw & Packaging Materials
Apply effective controls for receipt, identification, storage, segregation, handling, and traceability of materials.
Production Controls
Understand controlled manufacturing, batch processing, in-process checks, and practices that protect product consistency and integrity.
Quality Control & Laboratory Practices
Learn how sampling, testing, laboratory controls, and product release activities support cosmetic product quality and safety.
Finished Product Management
Understand identification, release, storage, handling, and traceability requirements for finished cosmetic products.
Non-Conforming Products
Learn how to identify, segregate, investigate, assess, rework, reprocess, reject, or dispose of non-conforming products.
Waste Management
Apply controlled waste segregation, collection, storage, handling, and disposal practices within GMP environments.
Deviations & Corrective Actions
Understand how deviations are documented, investigated, risk-assessed, and addressed through appropriate corrective actions.
Complaints & Product Recalls
Learn structured processes for complaint investigation, product traceability, recall management, and consumer protection.
Subcontracting & External Providers
Understand how outsourced GMP activities and external providers should be controlled and monitored.
Change Control & Risk Management
Evaluate and manage changes that may affect product quality, safety, manufacturing controls, or GMP compliance.
Documentation & Internal Audits
Maintain inspection-ready records and use internal audits to identify gaps, verify compliance, and drive continual improvement.
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