Attentive to the constant evolution of regulatory requirements, our entire team is fully committed to a
global comprehensive Quality Policy.
In response to your project needs, we strive to continuously improve our services with a completely
transparent approach.
Our Quality Department adheres to an extremely operational approach
A pharmaceutical establishment licence including manufacturing, import and distribution activities
validated by the French competent authorits (Authorisation number MM18/144)
An effective Quality Assurance system that integrates the principles of risk management
A team regularly trained in GMP, GDP and GCP regulations
A policy of continuous improvement by means of internal and external auditsA team regularly trained in GMP, GDP and GCP regulations
Quality and regulatory services adapted to your needs
Quality control at key stages of pharmaceutical processes
Management of retention and reference samples
Qualification audits of service providers and manufacturers
Pharmaceutical Certification of your clinical batches by our Qualified Person
Regulatory Watch and related advice