Appletree CI Group is an expert niche CRO and global regulatory affairs service provider with track records in ophthalmology and medical device investigations. We are present in 11 European countries and have over 30 permanent staff. By having an in-depth understanding of local cultures and customs, as well as experience with national regulations we are able to facilitate your clinical development and regulatory projects. Contract services: - Clinical trials phases I-IV - site feasibility, evaluation and initiation - monitoring services, close out - submissions - Medical writing - Consulting - Clinical trial authorizations Europe - Marketing authorization applications - Life cycle management, variations management - Scientific advice