Pharmaceutical quality control analysis laboratory
Your needs: perform frequent quality control analysis on your pharmaceutical products
Whether for human or animal health, the pharmaceutical industry is one of the most regulated industries in the world.
Quality compliance, or quality control of drugs and other pharmaceutical products (raw materials, packaging), is an integral part of the manufacturing process before a pharmaceutical product is put on the market.
Since the implementation of the “Good Manufacturing Practices” (GMP), quality control tests appear throughout the manufacturing process, both at the reception of raw materials and at the release of a batch of medicine.
These quality control tests are defined according to specific guidelines such as the European or American pharmacopoeia.
Our solutions : to provide you with our skills and our analytical tools, adapting them to your pharmaceutical challenges.
FILAB offers pharmaceutical companies high-level human skills. Indeed, our perfect knowledge of the specificities of your sector allows us to offer you a tailor-made support according to your analysis needs. Our PhD students and specialized engineers are at your disposal at each step of the quality control process. Our state-of-the-art analytical equipment offers you services that meet your compliance criteria in compliance with regulatory standards and for all types of drugs and dosage forms.
In order to respond accurately and reliably to your problems, FILAB offers tailor-made support for the analysis of your drugs:
Our services
Determination of nitrosamines in pharmaceutical products
Analytical validation ICH Q2
Forced degradation studies on pharmaceutical products or packaging
Dissolution test
Custom chemical analysis on raw materials, finished products or packaging.
Research of elementary impurities according to USP 233 (ICH Q3D context)
Powder characterization and particle size analysis
Stability studies
Deformation of raw material or finished product
