Quality and Regulatory

Compliance: A Component of Quality

Toxikon Europe provides comprehensive analytical services for all stages of product development, from concept to final product. The scientific approach of our experienced staff provides comprehensive techniques for the pharmaceutical and biotechnology industries, including method development and validation, stability studies, extractables & leachables, microbiological and bioanalytical services. 

Our facilities and dedicated laboratory management can offer the highest quality of work in compliance with GMP, GLP OECD and ISO 17025. With decades of experience, our team will collaborate with you as an extension of your company to facilitate drug and device development, achieve product safety, regulatory compliance, as well as maintain the highest levels of laboratory quality control.

 

Toxikon compliance testing services

Toxikon Europe is recognized for the analysis and control of medicinal products, narcotics and homones by the Belgian Ministry of Health and has an in-house QP. This recognition means EU-GMP compliance.

Toxikon Europe laboratory is:

 

Toxikon R&D Services

In order to accommodate Sponsor’s request for Research & Development testing in early phase of drug development, Toxikon offers its services as part of their R&D.  Toxikon provides these services with the same qualified instruments and trained personnel. 

quality-regulatory
FDA, EPA, USDA, OECD, ICH, ISO 17025, quality and regulatory