Our team of scientists can assist in interpreting and understanding the requirements of animal health products under Directive 2001/82 and can manage the environmental aspects for medicinal products for human health under Directive 2001/83/EC.
TSGE has the ability to prepare complete or partial dossiers, carry out quality, safety and efficacy expert reports, complete risk assessments and monitor studies for the registration of products. We are also able to provide guidance on the strategy to be followed to obtain National and/or European registration in the shortest time. Our wide-ranging experience of other regulated chemical sectors supports our veterinary and human medicines service.
If you would like any further information on our services, please do not hesitate to contact us.