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Cosmetic Good Manufacturing Practice Regulations [Pre-sale]

  •   22 Aug 2019
  •    Ye Chen
  •  531
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    • Cosmetic Good Manufacturing Practice Regulations [Pre-sale]

    • Language:EN/CN
    • Format:Electronic Edition (Adobe PDF)
    • Pages:
    • Translated by: ChemLinked
    • Publish date: 2019-08-22
    • Price: $370  (Free for premium members)

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    This product is for pre-sale! Please contact us at cosmetic@chemlinked.com for the details of the translation.
    This product is about Cosmetic GMP regulations in Taiwan. 
    1. Define all the special terms in this regulation, such as Out-of-specification, consumable and etc
    2. Specified Cosmetic Categories Shall Comply with Cosmetics Good Manufacturing Practice Regulations
    3. The requirements and responsibilities for cosmetic managers and practitioners
    4. Plant and facilities, including lighting, ventilation and etc
    5. Requirements for using Ingredients and packaging
    6. Requirements during manufacturing process
    7. Requirements for dealing with finished products, such as storage requirements and transportation requirements
    8. Requirements for quality control laboratory
    9. The disposal of out-of-specification products
    10. The disposal of waste
    11. Requirements for entrusted manufacturers
    12. Deviation processing
    13. Complaints and recalling
    14. Internal audit: manufacturers should conduct internal audit regularly or unregularly.
    15. Build a documentation system and make sure the readability of all documentations.
    16. Other rules
    Chapter 1: General Principles
    Chapter 2: Management and Practitioner
    Chapter 3: Factory and Facilities
    Chapter 4: Equipment
    Chapter 5: Ingredients and Packaging
    Chapter 6: Manufacture
    Chapter 7: Finished Products
    Chapter 8: Quality Control Laboratory
    Chapter 9: Disposal of Products That Do Not Meet Specifications
    Chapter 10: Disposal of Waste
    Chapter 11: Entrusted Work
    Chapter 12: Deviation Processing
    Chapter 13: Complaint and Recall
    Chapter 14: The Change of Regulation
    Chapter 15: Internal Audit
    Chapter 16: Documented
    Chapter 17: Supplementary
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