Online Training: IUCLID for Plant Protection Products: A Hands-on Guide

You will learn

• about the basic characteristics and functions of the IUCLID Software
• how to use IUCLID for submissions in the working context of PPPs
• how to complete a study record for each IUCLID Section

Monday, 9 December 2024 | 9:00 – 13:00 CET

Basic and general characteristics of the IUCLID software

Scope of the software, download, differences in local, server and cloud instalments
User, legal entity and rights
General elements of the software, meaning of the different entities:

• Substance
• Dossier
• Mixture/Product
• Reference substance
• Test material
• Templates
• Literature

IUCLID – Basic functions

• Creation of the different entities: mandatory and optional fields
• Difference and compilation of the different sections between endpoint and summaries
• Key study, supporting study
• QSAR, QMRF, QPRF
• Data waiving, importing, exporting and backups

Tuesday, 10 December 2024 | 9:00 – 12:00 CET

IUCLID for the different submissions

• Working contexts for PPPs
• Confidentiality and sanification
• Reports
• Validations
• Attachments, LoA and other documents
• Creation and submission of the dossier

Practical case

• Compilation of a study record for each IUCLID section
• Tips and tricks

Questions & Answers

End of the online training

Who should attend this training?

Professionals working in the fields of:

• Regulatory affairs
• Registration
• Exposure assessment
• Risk assessment
• Toxicology

Sectors that should take part:

• Plant protection industry
• Scientific and regulatory consultancies