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GMP for cosmetics Course & Certification
Intermediate
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97% Recommended
3 hour
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About
The GMP for Cosmetics Course & Certification is designed to provide a practical understanding of Good Manufacturing Practice (GMP) principles applied to the cosmetic and personal care industry. The course focuses on ensuring product safety, quality, and regulatory compliance throughout the manufacturing lifecycle.
This course covers cosmetic GMP guidelines, hygiene and sanitation practices, raw material control, production and packaging processes, quality assurance systems, documentation requirements, and contamination prevention. It also emphasizes regulatory expectations, audit readiness, and best practices for maintaining consistent product quality. Upon successful completion, learners receive a certification demonstrating competency in GMP for cosmetics manufacturing.
Who Should Enrol?
- Cosmetic Manufacturing Professionals
- Quality Assurance and Quality Control Teams
- Production and Operations Staff
- Regulatory Affairs Professionals
- Formulation and R&D Scientists
- Cosmetic and Personal Care Industry Employees
- Life Science, Pharmacy, Chemistry, and Engineering Graduates
What you will learn
Understand the fundamentals of GMP for cosmetics, including ISO 22716 requirements and their role in ensuring product safety and quality.
Learn the core elements of a cosmetic Quality Management System, including personnel training, hygiene, premises, equipment, and supplier control.
Gain knowledge of production and quality control processes, including raw material management, testing, documentation, and record keeping.
Develop an understanding of cosmetovigilance, complaint handling, recalls, audit readiness, and inspection preparedness to ensure regulatory compliance and consumer safety.
Course Syllabus
- Introduction to Cosmetics GMP + ISO 22716
- Concepts (part 1)
- Concepts (part 2)
- A private-label brand's first factory audit
- What inspectors look for
- What would you do?
- The 15-clause operating map
- Top mistakes + risks
- Key points to carry forward
- Quality Management System for Cosmetics
- Concepts (part 1)
- Concepts (part 2)
- Inside a mid-size contract manufacturer's QMS
- What inspectors look for
- What would you do?
- QMS documentation pyramid — what lives where
- Top mistakes + risks
- Key points to carry forward
- Personnel + Training
- Concepts (part 1)
- Concepts (part 2)
- Induction day at a skincare factory
- What inspectors look for
- What would you do?
- Training matrix — one row per role
- Top mistakes + risks
- Key points to carry forward
- Premises + Equipment
- Concepts (part 1)
- Concepts (part 2)
- Walking a skincare factory with an auditor
- What inspectors look for
- What would you do?
- Equipment qualification — IQ/OQ/PQ in cosmetics
- Top mistakes + risks
- Key points to carry forward
- Raw Materials + Supplier Management
- Concepts (part 1)
- Concepts (part 2)
- A raw material failure, caught
- What inspectors look for
- What would you do?
- Supplier qualification — minimum evidence bundle
- Top mistakes + risks
- Key points to carry forward
- Production + Process Control
- Concepts (part 1)
- Concepts (part 2)
- A campaign change on a colour-cosmetics line
- What inspectors look for
- What would you do?
- Line clearance checklist — 7 critical points
- Top mistakes + risks
- Key points to carry forward
- Quality Control + Testing
- Concepts (part 1)
- Concepts (part 2)
- Batch release, end-to-end
- What inspectors look for
- What would you do?
- Finished product release — specification + testing
- Top mistakes + risks
- Key points to carry forward
- Documentation + Record Keeping
- Concepts (part 1)
- Concepts (part 2)
- A batch record done right
- What inspectors look for
- What would you do?
- CAPA workflow — how a good one runs
- Top mistakes + risks
- Key points to carry forward
- Complaints, Recalls + Cosmetovigilance
- Concepts (part 1)
- Concepts (part 2)
- A complaint, worked end-to-end
- What inspectors look for
- What would you do?
- Recall playbook — eight steps
- Top mistakes + risks
- Key points to carry forward
- Audits + Inspection Readiness
- Concepts (part 1)
- Concepts (part 2)
- A Thursday audit — walked well
- What inspectors look for
- What would you do?
- Top audit findings — and how to close them
- Top mistakes + risks
- Key points to carry forward
- How this assessment works
- Scoring + the credential
- What your Certificate of Completion delivers
- Apply the course — the first 30 days
- Completion Slide
Course Benefits
Fully compliant
This course follows the guidance of Annex 13 of the European Commission's GMP guidelines
Certified
All learners who pass the final exam receive a uniquely numbered, personal certificate to demonstrate their subject knowledge. Since the questions are picked randomly from a database, re-sitting the exam doesn’t mean taking the same questions again and again.
Affordable
Our cost-effective prices represent excellent value. You can easily pay up to ten-times more for face-to-face training. We can also offer generous group discounts on larger purchases.
Time-saving
Our new administration system makes it incredibly quick and simple to allocate licences to multiple learners. Learners save time too by choosing when and where they complete the training. Our reporting tools make it easy for administrators to check the progress of learners and identify areas for future training.
Reliable and trustworthy
This course was written by McCarthy Consultant Services Inc (Canadian specialists in regulatory work to support the global pharmaceutical, biotechnology, medical device, food, natural health products and cosmetic industries). You will also stay up to date with any legislative changes in GMP relating to IMPs as our training courses are constantly monitored, reviewed and updated.
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