At Richard Vesely based in Laren, North-Holland, we specialise in EU medicine regulation. We provide regulatory advice about the development of medicine to various pharmaceutical companies and academic institutions. With 15 years of experience in different leading positions at the European Medicines Agency and at the global drug development service organisation we are able to provide insight into various regulatory requirements and help to find the best way forward for medicine to reach its customers and help patients around the world who need it.
Role within INTERCEPT
Richard Vesely is providing regulatory consultancy for the INTERCEPT project. They are responsible for tasks related to research ethics and interaction with regulators. They will also be consulted for various aspects of the clinical study protocols.
Main contacts
Dr Richard Vesely
Owner, consultant