Focuses on showcasing FAIR data collections through the use of dashboards, highlighting how persistent identifiers (PIDs), well-structured metadata, and institutional data presentation can enhance transparency, accessibility, and reuse.

Presents the use of salivary leukocytes as a non-invasive biomatrix for assessing DNA damage and repair in biomonitoring studies using the comet assay, including methodological optimization and validation of both fresh and cryopreserved samples.

An in-depth look at the development and validation of QSAR models for chemical risk assessment, covering molecular descriptors, statistical modeling techniques, applicability domains, and the principles guiding regulatory acceptance.

An overview of in silico approaches in PARC, highlighting VEGA software and integrated platforms for assessing chemical properties aligned with SSbD principles.

This webinar explores the exposome framework in toxicology, focusing on multi-stressor interactions, long-term effects, and regulatory implications for environmental health.

ECHA’s approach to group substance assessments, upcoming improvements in communication to registrants, and how to respond if your substance is included.

Slide-based resource on OECD test guidelines, supporting science-regulation knowledge transfer, harmonisation, and onboarding of new Test Guideline developers (comtains 4 different modules).

An overview of risk assessment methodology, emphasizing the steps from hazard identification to exposure characterization and the use of scientific evidence in defining safety thresholds.

A European perspective on workplace risk assessments, featuring presentations on legislation, behavioral approaches, and the OiRA tool to support micro and small businesses.

Covers key features and future plans for the QSAR Toolbox, including integration with IUCLID and applications in non-animal hazard assessment.

Explores the concept, misconceptions, and future potential of AOPs in predictive toxicology, featuring case studies from nanosafety and discussing their integration with data-driven and high-throughput strategies.

Focuses on risk assessment of combined chemical exposures, highlighting approaches like AOPs, TK/TD models, and in silico methods for regulated products and contaminants.

Focuses on addressing FAIR data challenges in research, highlighting persistent identifiers, metadata, and semantic interoperability through expert presentations and interactive discussions.

A practical guide to navigating FAIR principles, drafting Data Management Plans, and sharing research outcomes, tailored to the needs of diverse research stakeholders.

Presents the RACE tool, supporting exposure assessment for food contaminants by comparing intake estimates with health-based guidance values.

A deep dive into FAIRsFAIR’s work on metadata, semantic interoperability, and persistent identifiers, with insights into aligning technical solutions across European research infrastructures.

This presentation focuses on the molecular pathways involved in the development of asbestos-related diseases, emphasising the roles of oxidative stress, DNA repair, and xenobiotic metabolism. It explores how both germline mutations and single-nucleotide polymorphisms (SNPs) within these pathways influence individual susceptibility. By understanding these mechanisms, researchers can identify clinically relevant biomarkers that support early diagnosis and risk assessment.