Your needs: validate your analytical methods and assays in accordance with your regulatory requirements
In order to optimize your existing products, to launch new products or even in the context of a regulatory change, the development of customized analytical methods allows you to perform specific analysis on your matrices.
Whatever your field of activity, analytical validation consists of guaranteeing the performance of an analytical method by examining and providing objective evidence, with regard to the expected use of the product. It also allows to estimate its measurement uncertainties.
However, the validation of specific methods is particularly complex because several parameters must be taken into account. Indeed, specificity, repeatability, reproducibility and linearity are the main parameters to study.
Thus, the validation of your analytical methods and assays by a competent laboratory is a considerable asset.
Our solutions: FILAB assists you with all your analytical and dosing method validation needs
FILAB supports you in the validation of your analytical and dosing methods and also takes charge of the various stages of implementation.
With its high level of in-house expertise and diversified analytical equipment, FILAB analyzes your needs and offers you solutions adapted to the standards associated with your problem.
our technical means
Gas chromatography coupled with mass spectrometry GC-MS
ICP coupled to mass spectrometry ICP-MS ICP-AES / ICP-OES
FTIR microscopy
Ion chromatography CI
Liquid Chromatography-Mass Spectrometry LC-MSMS
X-ray diffraction DRX
Differential Scanning Calorimetry DSC
In addition, FILAB assists you in the validation of analytical methods and assays according to specific standards and guidelines:
Analytical validation according to ICH Q2
Method validation according to USP 1225
Method validation according to SANCO 30/30
Method validation according to NF T90-210
Method validation according to ANVISA
