Pharma and Biotech

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

Our facilities and experienced laboratory management can offer the highest quality of work in compliance with cGMP, 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.  By partnering with us and learning your application, Toxikon provides customized solutions which will facilitate your development.

 

ISO 17025 Certified, GMP Recognized, GLP Monitored and FDA Registered. 

BioPharma