Evoluation
The evaluation phase within REACH is subsequent to the registration one. There are two types of evaluation:
1. Dossier Evaluation ...
Authorisation
The aim of the Аuthorization process within the Regulation consists in promoting the gradual substitution of dangerous substances, weather it is technologically and technically viable. The substances which fall under the authorization...
Restriction
The Restrictions procedure allows the competent authority of the Member State (Ministry of environment and water) and ultimately the EU Commission to restrict the placing on the market and the use of certain substances, which...
Substances in articles
Under the Regulation, substances in articles have an obligation of registration if the following conditions are met:
v the substance is intended to be released during normal and reasonable foreseeable...
Scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD)
You can find information in the Guidance of PPORD see Full text (ENG).
