The Regulatory Information System (RIS) is currently undergoing redevelopment and is not available to external visitors. It will return as a more user-friendly, interactive digital platform soon.
RIS was developed jointly by EATRIS and CZECRIN. It is managed and regularly updated by CZECRIN’s regulatory specialists.
EATRIS Regulatory Database is a free-of-charge service that contains information about the regulatory requirements, guidelines and legislation from 27 EU countries (as well as Norway, Switzerland, Turkey and Israel) regarding drug and medical device development derived from the application of European legislation.
