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Veterinary medicinal products

ERA (Environmental Risk Assessment)
For the authorisation of your veterinary medicinal product in accordance with the requirements of the European Medicines Agency (EMEA, according to CVMP/ERA/418282/2005-Ref.1), an Environmental Risk Assessment (ERA) consisting of 2 phases is required. In the so-called Phase II, the effects of the veterinary medicinal products on the environment are examined.
We advise you in the following areas:

- + 49 30 843 13 661
- info@toxlicon.com
Find out more about our services
We offer a comprehensive range of services that includes scientific and regulatory consulting, the development of test strategies for regulatory approvals, test and project support and the commissioning of laboratories.We also provide support with professional study monitoring for GLP studies and the preparation of complete authorisation dossiers. Our services can be flexibly tailored to your needs and can be utilised either individually or as a customised overall package.
Scientific and regulatory advice
Test strategy for regulatory approval
Test and project support
Laboratory commissioning
Study monitoring of GLP studies
Dossier creation

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- + 49 30 843 13 661
- info@toxlicon.com