1. The competent authorities, the Agency and the Commission shall have full access to the information in the product database.
2. Marketing authorisation holders shall have full access to the information in the product database as regards their marketing authorisations.
3. The general public shall have access to information in the product database, without the possibility to change the information therein, as regards the list of the veterinary medicinal products, the summary of product characteristics, package leaflets and, after the deletion of any commercially confidential information by the competent authority, assessment reports.