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Regulatory Strategy


Are you launching your cosmetics in the EU?

Regulations can be a 'Beast'!

Protect your 'Beauty' Cosmetics with a robust regulatory Strategy!


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Representation to the EC


We shall act as your Responsible Person to the European Commission and help you place your cosmetics on the EU market.


Your Regulatory First Responders in the EU!


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Technical Documentation and Review


Our experts will support your product and ensure complete compliance with necessary regulations.

Bring your Cosmetics to EU with

Med-Di-Dia as your Regulatory Risk Partner!


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With over 25+ years of experience, our experts have successfully helped 115 cosmetics companies with complete regulatory compliance in the EU.

Come to us for one-stop regulatory support and representation for your cosmetics in the EU and around the world!


Our Broad range of Services:

  • EU Representation.
  • Register you on ECAS (European Commission Authentication Service) and SAAS (Sanco Authentication and Authorisation System).
  • Assess your existing Product Information Files (PIFs).
  • Carry out notifications on the CPNP on your behalf.
  • Provide guidance on permitted claims for cosmetic products.
  • Provide guidance on labelling requirements (including label review).
  • Compile Product Information Files (PIFs) including the Cosmetic Product Safety Report (CPSR).
  • Provide advice regarding Good Manufacturing Practice (GMP).
  • Advise on your Regulatory Strategy.
  • Offer advice and guidance re International Nomenclature for Cosmetic Ingredients (INCI).
  • Provide an annual surveillance service.
  • Assess your advertising and marketing materials.

Looking for regulatory support outside the EU? Click on the Link Below!


Rest of World regulatory and quality compliance expertise is provided by our parent company, Global Regulatory Services (GRS).


Risk Management Analysis (ISO 14971:2019)

Risk Management Analysis (ISO 14971:2019)

Medical Device Manufacturers have a legal obligation to regularly maintain and perform risk management analyses.


Patient information management (IFU, Labelling and Cartons)

Patient information management (IFU, Labelling and Cartons)

A ‘Label’ is the identity of the product.


Unique Device Identification (UDI) & Global Unique Device Identification Database (GUDID)

Unique Device Identification (UDI) & Global Unique Device Identification Database (GUDID)

It allows the identification of specific devices on the market and facilitates their traceability.