Cosmetics

cosmetics

Cosmetics

In India, the CDSCO regulates and controls the import of Beauty and Personal Care Products under the Drugs and Cosmetics Act and Cosmetics Rules 2020. We offer our clients complete assistance,planning and review of the various processes of import of cosmetics or import of new cosmetics or import of cosmetics already registered in India. Our experts have many years of experience in carrying out cosmetics import and registration,certification and manufacturing permission thereby, making us your best partner in guiding you through the entire regulatory and compliance process.

We offer the following services, helping you to navigate the cosmetic regulations in India-

  1. Cosmetics Import and Registration-
  • Form COS-1
  • Form COS-2
  • Form COS-3
  • Form COS-4 &4A
  • Form COS-12

 

  1. To Manufacturers (India)-
  • Form COS 8- License to Manufacture Cosmetics for sale or distribution (Application in Form COS-5)
  • Form COS 9- Loan License to Manufacture Cosmetics  for sale or distribution (Application in Form COS-6)
  • Form COS 23 – Approval for carrying out test on cosmetics and raw materials used in thier manufacturing on behalf of licensees( Application in Form COS 22)
  1. To Importers(Authorised agent)- Registration of Indian Authorised Agent (IAA) on SUGAM portal.
  2. Label Review-

We offer labelling assistance as per the Cosmetics Labelling Regulations, Cosmetic Rules, 2020 and Legal Metrology (Package Commodities) Rules 2011 and full guidance for the labelling of imported cosmetics in India.

  1. Cosmetic Product Testing-

We offer cosmetics product testing in consonance with the Bureau of Indian Standards (BIS) requirements through our various state FDA and CDSCO certified labs all over India.

 

Regulation/Guidelines

Medical Devices in European Union(EU)

Medical devices are products or equipment intended for a medical purpose. In the European Union (EU) they must undergo a conformity assessment to demonstrate they meet legal requirements to ensure they are safe and perform as intended. They are regulated at EU Member State level, but the E...

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October 31st, 2021
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What's New ?
  • Regulation/Guidelines
    Medical Devices in European Union(EU)

    Medical devices are products or equipment intended for a medical purpose. In the European Union (EU) they must undergo a conformity assessment to demonstrate they meet legal requirements to ensure they are safe and perform as intended. They are regulated at EU Member State level, but the E...

    October 31st, 2021