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This book summarizes the authority of regulatory agencies and programs as they pertain to the cosmetic industry, offers practical advice on how to operate within the regulatory environment, and introduces scientific and regulatory issues that are likely to have an impact on cosmetic manufacturers.
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This book summarizes the authority of regulatory agencies and programs as they pertain to the cosmetic industry, offers practical advice on how to operate within the regulatory environment, and introduces scientific and regulatory issues that are likely to have an impact on cosmetic manufacturers.
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Produktdetails
- Produktdetails
- Verlag: Taylor & Francis Ltd (Sales)
- Seitenzahl: 720
- Erscheinungstermin: 2. Dezember 2019
- Englisch
- Abmessung: 231mm x 152mm x 43mm
- Gewicht: 1089g
- ISBN-13: 9780367451769
- ISBN-10: 036745176X
- Artikelnr.: 58440118
- Verlag: Taylor & Francis Ltd (Sales)
- Seitenzahl: 720
- Erscheinungstermin: 2. Dezember 2019
- Englisch
- Abmessung: 231mm x 152mm x 43mm
- Gewicht: 1089g
- ISBN-13: 9780367451769
- ISBN-10: 036745176X
- Artikelnr.: 58440118
Estrin,
Part I: The Regulatory Environment 1. Regulation of Cosmetics in the United
States: An Overview 2. The FDA's Scientific and Regulatory Programs for
Cosmetics 3. The Toxic Substances Control Act and Its Potential Impact on
the Cosmetic Industry 4. Federal Regulation of Soap Products 5. The Impact
of the FDA's Over-the-Counter Drug Review Program on the Regulation of
Cosmetics 6. Regulation of Advertising by the Federal Trade Commission 7.
The Impact of Other Regulatory Agencies on the Cosmetic Industry 8. An
Overview of Worldwide Regulatory Programs 9. Cosmetics: The Legislative
Climate Part II: Functioning in the Regulatory Environment 10. Voluntary
Self- Regulation Programs of the Cosmetic Industry 11. Organization for
Action-Development of CTFA's Scientific Programs 12. The Cosmetic
Ingredient Review 13. The Industry Response Program to the Cosmetic
Ingredient Review 14. The RIFM Story 15. Cosmetic Industry Research
Programs 16. Industry Programs for Dealing with Trace Contaminants 17. The
Johns Hopkins Center for Alternatives to Animal Testing 18. Communication
and Cooperation -The Dermatologist and the Cosmetic Industry 19. Industry
Performance and Public Opinion: Some Reflection on Public Relations 20.
Preparing for Cosmetic GMPs 21. Evaluating Your Microbiology Program 22.
Establishing a Training Program for Plant Personnel 23. Coping with
Cosmetic Labeling 24. The CTFA Cosmetic Ingredient Dictionary 25. Coping
with the Color Additive Regulations 26. Adequately Substantiating the
Safety of Cosmetic and Toiletry Products 27. Managerial and Technical
Responsibilities for Selecting a Laboratory for GLP Toxicology Studies 28.
Ocular Irritancy: The Search for Acceptable and Humane Test Methods 29.
When an FDA Inspector Calls 30. How and When to Recall 31. Establishing a
Consumer Response Program 32. Special Problems of Small Companies 33. The
Private Label Company-Special Considerations 34. Innovating in a Regulated
Environment Part III: Challenges for Tomorrow 35.
States: An Overview 2. The FDA's Scientific and Regulatory Programs for
Cosmetics 3. The Toxic Substances Control Act and Its Potential Impact on
the Cosmetic Industry 4. Federal Regulation of Soap Products 5. The Impact
of the FDA's Over-the-Counter Drug Review Program on the Regulation of
Cosmetics 6. Regulation of Advertising by the Federal Trade Commission 7.
The Impact of Other Regulatory Agencies on the Cosmetic Industry 8. An
Overview of Worldwide Regulatory Programs 9. Cosmetics: The Legislative
Climate Part II: Functioning in the Regulatory Environment 10. Voluntary
Self- Regulation Programs of the Cosmetic Industry 11. Organization for
Action-Development of CTFA's Scientific Programs 12. The Cosmetic
Ingredient Review 13. The Industry Response Program to the Cosmetic
Ingredient Review 14. The RIFM Story 15. Cosmetic Industry Research
Programs 16. Industry Programs for Dealing with Trace Contaminants 17. The
Johns Hopkins Center for Alternatives to Animal Testing 18. Communication
and Cooperation -The Dermatologist and the Cosmetic Industry 19. Industry
Performance and Public Opinion: Some Reflection on Public Relations 20.
Preparing for Cosmetic GMPs 21. Evaluating Your Microbiology Program 22.
Establishing a Training Program for Plant Personnel 23. Coping with
Cosmetic Labeling 24. The CTFA Cosmetic Ingredient Dictionary 25. Coping
with the Color Additive Regulations 26. Adequately Substantiating the
Safety of Cosmetic and Toiletry Products 27. Managerial and Technical
Responsibilities for Selecting a Laboratory for GLP Toxicology Studies 28.
Ocular Irritancy: The Search for Acceptable and Humane Test Methods 29.
When an FDA Inspector Calls 30. How and When to Recall 31. Establishing a
Consumer Response Program 32. Special Problems of Small Companies 33. The
Private Label Company-Special Considerations 34. Innovating in a Regulated
Environment Part III: Challenges for Tomorrow 35.
Part I: The Regulatory Environment 1. Regulation of Cosmetics in the United
States: An Overview 2. The FDA's Scientific and Regulatory Programs for
Cosmetics 3. The Toxic Substances Control Act and Its Potential Impact on
the Cosmetic Industry 4. Federal Regulation of Soap Products 5. The Impact
of the FDA's Over-the-Counter Drug Review Program on the Regulation of
Cosmetics 6. Regulation of Advertising by the Federal Trade Commission 7.
The Impact of Other Regulatory Agencies on the Cosmetic Industry 8. An
Overview of Worldwide Regulatory Programs 9. Cosmetics: The Legislative
Climate Part II: Functioning in the Regulatory Environment 10. Voluntary
Self- Regulation Programs of the Cosmetic Industry 11. Organization for
Action-Development of CTFA's Scientific Programs 12. The Cosmetic
Ingredient Review 13. The Industry Response Program to the Cosmetic
Ingredient Review 14. The RIFM Story 15. Cosmetic Industry Research
Programs 16. Industry Programs for Dealing with Trace Contaminants 17. The
Johns Hopkins Center for Alternatives to Animal Testing 18. Communication
and Cooperation -The Dermatologist and the Cosmetic Industry 19. Industry
Performance and Public Opinion: Some Reflection on Public Relations 20.
Preparing for Cosmetic GMPs 21. Evaluating Your Microbiology Program 22.
Establishing a Training Program for Plant Personnel 23. Coping with
Cosmetic Labeling 24. The CTFA Cosmetic Ingredient Dictionary 25. Coping
with the Color Additive Regulations 26. Adequately Substantiating the
Safety of Cosmetic and Toiletry Products 27. Managerial and Technical
Responsibilities for Selecting a Laboratory for GLP Toxicology Studies 28.
Ocular Irritancy: The Search for Acceptable and Humane Test Methods 29.
When an FDA Inspector Calls 30. How and When to Recall 31. Establishing a
Consumer Response Program 32. Special Problems of Small Companies 33. The
Private Label Company-Special Considerations 34. Innovating in a Regulated
Environment Part III: Challenges for Tomorrow 35.
States: An Overview 2. The FDA's Scientific and Regulatory Programs for
Cosmetics 3. The Toxic Substances Control Act and Its Potential Impact on
the Cosmetic Industry 4. Federal Regulation of Soap Products 5. The Impact
of the FDA's Over-the-Counter Drug Review Program on the Regulation of
Cosmetics 6. Regulation of Advertising by the Federal Trade Commission 7.
The Impact of Other Regulatory Agencies on the Cosmetic Industry 8. An
Overview of Worldwide Regulatory Programs 9. Cosmetics: The Legislative
Climate Part II: Functioning in the Regulatory Environment 10. Voluntary
Self- Regulation Programs of the Cosmetic Industry 11. Organization for
Action-Development of CTFA's Scientific Programs 12. The Cosmetic
Ingredient Review 13. The Industry Response Program to the Cosmetic
Ingredient Review 14. The RIFM Story 15. Cosmetic Industry Research
Programs 16. Industry Programs for Dealing with Trace Contaminants 17. The
Johns Hopkins Center for Alternatives to Animal Testing 18. Communication
and Cooperation -The Dermatologist and the Cosmetic Industry 19. Industry
Performance and Public Opinion: Some Reflection on Public Relations 20.
Preparing for Cosmetic GMPs 21. Evaluating Your Microbiology Program 22.
Establishing a Training Program for Plant Personnel 23. Coping with
Cosmetic Labeling 24. The CTFA Cosmetic Ingredient Dictionary 25. Coping
with the Color Additive Regulations 26. Adequately Substantiating the
Safety of Cosmetic and Toiletry Products 27. Managerial and Technical
Responsibilities for Selecting a Laboratory for GLP Toxicology Studies 28.
Ocular Irritancy: The Search for Acceptable and Humane Test Methods 29.
When an FDA Inspector Calls 30. How and When to Recall 31. Establishing a
Consumer Response Program 32. Special Problems of Small Companies 33. The
Private Label Company-Special Considerations 34. Innovating in a Regulated
Environment Part III: Challenges for Tomorrow 35.