Dr Cemile Jakupoglu, Clinical Safety and Efficacy Executive at Cyton's office in Germany, will be at the "Symposium on the new European legislation on veterinary medicines", being held in Brussels, by the Belgian agency, FAMHP.
Cemile is ready to meet with established animal health companies to discuss Cyton's consultancy services in product development and registration, and with innovators seeking to understand the regulatory framework for their products.
Companies may also wish to discuss how they could be affected by Brexit and how Cyton can help. With offices in the UK and also in Germany, Cyton is ready to provide our current suite of services, with increased capacity, in the UK and the rest of Europe, after Brexit.
Please contact Cemile if you would like to meet at the event.
Regulatory Outsourcing Options
Cyton’s dedicated regulatory procedures team can support you with:
- Dossier preparation, submission & regulatory procedures
- Regulatory intelligence and strategic planning
- Life cycle management
- Key person cover
- Pharmacovigilance
- Brexit support services