Regulatory Services
Despite promises to the contrary the regulatory framework for providing clinical trials still remains complex. EastHORN Clinical Services in CEE can provide you with all the local regulatory expertise to ensure the smoothest possible start to your study in the CEE. We have a “start up” team dedicated to this service. As CEE countries move towards adopting the EU directives in Clinical Trials you can be reassured that EastHORN is keeping up with developments in each country and with each regulatory body.
Services# include
- Regulatory Board submissions
- Site Ethics Committee Submissions
- Site & Investigator Contracts
- Study materials (see Medical Writing section more details)
- Pharmacovigilance
#Language translations can be provided for each country
Contact regulatory@easthorn.eu for more information on our range of services