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Forced degradation study in laboratory
Your needs: to carry out a forced degradation study on a pharmaceutical product or on an active ingredient (API) within the framework of a pharmaceutical development
A forced degradation study or stress study is a stability test that simulates the evolution of the behavior of a pharmaceutical product or an active ingredient (API). The objective is to highlight the stability of a substance or drug over time and to observe the effects on its purity and compliance.
These forced degradation tests can be performed on active ingredients or on finished products.
Are you looking for a reliable and responsive laboratory for your forced degradation studies? Call on FILAB!
Our solutions: to accompany you in your stability tests and more particularly in the study of forced degradation of your pharmaceutical products
The FILAB laboratory offers stability and forced degradation studies on your pharmaceutical products as part of an R&D project or during quality control. Thanks to our 2,100m² analytical facilities, FILAB can provide the following services
Stability and forced degradation study according to ICH Q1A
Analysis of the chemical composition of the product according to specific environmental conditions (temperature, humidity, light exposure...) by GC-MS, HPLC or FTIR
Study of container-content interactions
Analysis of active ingredients
Deformation of pharmaceutical products
Custom chemical analysis to study the stability of a product
Method development and validation
Analysis and identification of impurities
Analysis and determination of degradation products
In order to assist you in the best conditions, FILAB laboratory is approved for Research Tax Credit (CIR).
For more information on our forced degradation studies, please contact us: email@example.com – tel: 03.80.52.32.05 or ask for a quote here.