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SYNLAB pharma supports all stages of the production process of cosmetics

We offer:

  • Consultancy for analytics and quality control
    -Physico chemical methods
    -Microbiological tests
    -Stability tests
  • Quality controls according to EP, USP or costumer requirements
  • Method transfer, verification and validation of analytical procedures
  • Clinical studies
  • Stability studies under defined climate conditions
  • In-use-stability


By definition in German legislation (LFGB Lebensmittel- und Futtermittelgesetzbuch), cosmetics are substances made for cleaning/washing the body surface like soaps or shampoos , for health protection like fluids and lotions and for modifying the look or the body odor like make-up or fragrances. The law also protects the customer against falsifications and potentially hazardous products. The names and declarations of the ingredients are regulated.

A new European guideline (1223/2009 (EG)) has been introduced in July 2013. The aim is to ensure customers safety at all times when using cosmetic products in the intended way. Similar to pharmaceutical products, GMP is the applicable guideline for the production process.


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Fellbach wird neuer Laborstandort
Nach zweijähriger Planungs- und Umbauphase entstand in Fellbach das neue Labor der SYNLAB Analytics & Services Germany GmbH.
Aug 10, 2018 Continue
Determination of the Impurity N-Nitroso dimethyl amine (NDMA) in Drug Substances with GC-MS

Due to contamination of a drug substance with the potential mutagenic substance N-Nitroso dimethyl amine (NDMA) a massive recall campaign was initiated for the related drug products. SYNLAB Pharma offers a GC-MS test for testing the absence of NDMA in drug substances and drug products.

Please contact our experts.

Jul 13, 2018 | Pharma Continue
New Services in Regulatory Compliance for Biologics

With immediate effect, SYNLAB Pharma provides a broad support in the field of Regulatory Compliance of Biologics development. With this new services we support specifically start-ups, small to medium sized biotech companies, which require professional consultancy and project execution in regulatory project design.

For further questions, please contact:

Jun 18, 2018 | Pharma Continue
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