Rivendell offers a broad range of services to our clients:
Regulatory consultancy on specific data requirements and all types of registration for all EU and Eastern European countries Click here for more details
Project management of complete registration programmes from generation of data by testing (toxicology, field trials, analytical chemistry) to dossier submission and follow-up until approval Click here for more details
Review of active substance and formulation data for completeness (data gap analysis) to determine the need for further data prior to registration Click here for more details
Preparation of notifications for the second and third priority lists of active substances under review according to Directive 91/414/EEC Click here for more details