Data Reviews for submission to ACVM

        Production of Technical dossiers 

        Prepare Summaries of efficacy and/or residue dossier 

        Registration requirements for ACVM and EPA

2.      MANAGEMENT OF RESEARCH PROGRAMMES

         Advise on NZ Government requirements for registration 

         Coordinate with field contract research organisations to provide best outcomes 

         Draft test protocols (for efficacy trials and GLP residue studies) 

         Monitor critical phases and provide on-site inspections Draft final reports 

         Disease, pest, weed, crop and yield assessments 

         Harvest monitoring 

         Advice on appropriate crop spray programmes 

4.      VINIFICATION STUDIES

        Liaison with wineries so that grape trials requiring winemaking meet the necessary industry requirements. 

        Provide independent wine tasting by suitably industry-recognised professionals ensuring they are conducted to a high standard.