Regulatory Affairs
Preparation and presentation of complete dossiers for product registration in accordance with national directives
and laws (plant protection product law, biocidal product law, etc.) for Austria and Germany.

Preparation and presentation of complete dossiers for the registration of new active substances respectively
the evaluation of existing active substances within the framework of Regulation (EC) No. 1107/2009.

  • Completeness Check
  • CA/CP dossiers for chemical active substance and product
  • MA/MP dossiers for microbiological active substance and product
  • Supporting documents such as data for formulants etc.
Preparation and presentation of complete dossiers for the registration of biocidal products according to national
directives and laws (biocidal product law).

Preparation and presentation of files for, or as support of, the registration of biocidal substances and products
in accordance with the Regulation (EU) No.528/2012 concerning the placing of biocidal products on the market respectively

Classification and labelling of various chemicals such as plant protection products, fertilisers, pest control
products and other biocides as well as industrial chemicals according to national laws; preparation of material
safety data sheets.

Preparation of literature searches for chemical substances to obtain data on their toxicological and
ecotoxicological profile.

Commissioning and supervising of toxicological and ecotoxicological studies in co-operation with qualified
test facilities.
Biological Efficacy Testing
Carrying out and evaluation of field trials according to EPPO guidelines to support the registration in respect
of biological efficacy and phytotoxicity of plant protection products.

To conduct those efficacy trials our specialists are closely working together with Austrian farmers in order
to be able to select the best location for the experimental target (soil properties, weed pressure respectively
infection pressure of plant diseases etc).

Carrying out of the field part of residue trials.