Laboratory analysis of cleaning residue for the pharmaceutical industry

Are you looking to analyze cleaning residue on your finished products ?

The analysis of cleaning residue is an integral part of the good manufacturing practices (GMPs). These analyses are carried out as part of regulatory testing linked to quality assurance of pharmaceutical products and production procedures.

Risk assessment linked to cleaning residue is done to prevent cross contaminations or even the apparition of residue during the production process which could have a negative impact on the quality of pharmaceutical products.

The analysis of cleaning residue is essential when a change in the production process occurs.

Our solution : to assist producers of pharmaceutical products in analyzing cleaning residue

FILAB offers pharmaceutical industrialists with a high level of technical skill and a cutting-edge analytical fleet to provide them with services fulfilling their needs for product compliance.

FILAB laboratory is able to assist you in analyzing cleaning residue by providing the following services :

FILAB has ISO 17025 accreditation for the analysis of pharmaceutical products (ICH Q3D).

our services

  • Detection of analytical residue in finished products

  • Development and validation of cleaning procedures

  • Procedural audits

  • Detection of impurities : residual solvents, inorganic impurities, catalytic residue…

  • Analytical training relating to cleaning procedures

  • Creation of a register of impurities

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

Thank you !

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