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. |
