Introduction:
This training will provide you with the basic knowledge on how to make PPP-related submissions in IUCLID. 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 and how to complete a study record for each IUCLID Section.
Program:
The course will focus on the following topics:
Basic and general characteristics of the IUCLID software
- Scope of the software, download, differences in local, server and cloud instalments, how to manage different versions
- 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
- Overview of guidance and manuals
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
- Weight of Evidence
- QSAR, QMRF, QPRF
- Data waiving
- Read Across
- Importing, exporting and backups
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
- Q&A
To whom:
This course is aimed at professionals working in the fields of Regulatory affairs, Registration, Exposure assessment, Risk assessment and Toxicology in the sector of Plant protection industry and Scientific and regulatory consultancies.
Teacher/Speaker:
Monica Locatelli
Language:
Italian
(available in English upon request)
Duration:
8 hours
Cost:
800 €/person
