Laboratory analysis of pharmaceutical formulations

Why monitor the quality of your pharmaceutical formulations ?

The pharmaceutical industry is one of the more stringent industries in terms of regulations. For this reason, many industrial pharmaceutical producers, of products intended for either animal or human consumption, are faced with numerous quality requirements.Regulations surrounding the quality of pharmaceutical formulations are not just applied during a product’s lifecycle, but also during development and marketing phases. All these quality control tests on pharmaceutical formulations are referenced in Pharmacopeias (USP, EP).

The non-compliance of a pharmaceutical formulation (impurities, API/excipient interactions…) could cause the product to not be authorized to be put to market or to be called back.

Are you looking for a reliable and reactive for the analysis of pharmaceutical formulations ? Call on FILAB !

FILAB is able to assist you in analyzing the compliance of your pharmaceutical formulations

FILAB offers pharmaceutical industrialists with a high level of skill and a cutting-edge analytical fleet to provide services fulfilling their criteria in terms of compliance to standards relevant to all kinds of galenic pharmaceutical formulations.

FILAB laboratory is the only French laboratory to be ISO 17025 accredited ( accreditation n°1-1793) for the analysis of elemental impurities in pharmaceutical matrices and for the analysis of pharmaceutical formulations in accordance with GMPs.

To reliably and precisely resolve these problems, FILAB offers tailored support for the analysis of your pharmaceutical formulations :

  • Chemical analysis of your pharmaceutical formulations by GC-MS, LC-MS, ICP
  • Analysis of pharmaceutical formulations following ICH and VICH guidelines
  • Detection of elemental impurities in your pharmaceutical formulations by ICP-MS or ICP-AES
  • Analysis of particulates in your pharmaceutical formulations (troubleshooting) by MEB-EDX, FTIR, LC-MS/MS
  • Reverse engineering of your pharmaceutical formulations
  • Extractables and leachables (E&L) testing  

For more information about our analytical services relating to pharmaceutical formulations, feel free to contact us via email at, over the phone by calling +33 (0)3 80 52 32 05 or request a free quote online here.

The positive aspects of FILAB

  • A highly qualified team

  • Responsiveness in responding to and processing requests

  • A complete analytical park of 2100m²

  • Tailor-made support

Anaïs DECAUX Customer Support Manager
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