In establishing the list of information to be recorded in the registers, account has been taken of the fact that other sets of information - such as the environmental risk assessment, the scientific studies, including studies which demonstrate the safety of the product, including, where available, references to independent and peer-reviewed studies, and to methods for identification and detection, and all other information submitted by the notifier, methods and plans for monitoring the GMO(s) and for emergency response, and results of the post-market monitoring - are in principle accessible according to the relevant provisions of Directive 2001/18/EC, Regulation (EC) No 1946/2003 of the European Parliament and the Council of 15 July 2003 on transboundary movements of genetically modified organisms(2) and Regulation (EC) No 1049/2001 of the European Parliament and the Council of 30 May 2001 regarding public access to European Parliament, Council and Commission documents(3), and therefore need not be recorded.
Pri vzpostavitvi seznama informacij, ki jih je treba vnesti v registre, je treba upoštevati dejstvo, da so druge vrste informacij - kakor na primer ocena tveganja za okolje, znanstvene študije, vključno s študijami, ki dokazujejo varnost proizvoda, vključno s sklicevanjem na neodvisne študije in strokovne preglede, če so dostopni, ter metode za identifikacijo in odkrivanje in vse druge informacije, ki jih predloži prijavitelj, metode in načrti za spremljanje GSO in za ukrepe v primeru nesreče ter rezultate spremljanja po sproščanju - načeloma dostopne v skladu z ustreznimi določbami Direktive 2001/18/ES, Uredbe (ES) št. 1946/2003 Evropskega parlamenta in Sveta z dne 15. julija 2003 o čezmejnem gibanju gensko spremenjenih organizmov [2] in Uredbe (ES) št. 1049/2001 Evropskega parlamenta in Sveta z dne 30. maja 2001 o dostopu javnosti do dokumentov Evropskega parlamenta, Sveta in Komisije [3] ter jih zato ni treba vnesti v registre.