This Regulation here determines the contents of necessary documentation that will be used for purposes of evaluation of phytopharmaceutical products. This type of evaluation is done for the purpose of phytopharmaceutical product registration. The detailed content of required documentation, with all the data for the phytopharmaceutical product assessment, is prescribed in the Annex, which is part of this text. Good Laboratory Practice, toxicological tests, residues of agents in or on treated products and food and animal feed are all topics covered in this Regulation (see Annex for details).
Босния и Герцеговина · 2015-12-16