Our expertise
covers all therapeutic classes, product types and delivery routes.
We have experience of all types of EU regulatory submissions and
we routinely prepare Centralised and De-centralised authorisation
applications and MRL submissions.
Cyton offers expertise appropriate to the task, including:
- Chemistry
- Pharmacy
- Product development and manufacture
- Pharmacology
- Toxicology
- Environmental Sciences
- Immunology
- Veterinary clinical medicine
- Biotechnology
- Microbiology and parasitology
For more information on the range of services we provide, please
review the links on the left.
A Management Forum Event:
The Animal Health Autumn School: Working Through Veterinary Drug Development in the EU and USA
‘Gain a comprehensive understanding of the development process for veterinary medicines’
28 Sept – 2 Oct 2009 - Boston, USA
Chaired by Ray Harding
Click Here for more Details
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