Science Beyond regulatory compliance

Regulatory TOXICOLOGY

Introduction to Regulatory Toxicology and Risk Assessment for Human Health

Programme

Part 1 – Regulatory Toxicology – Overview
Part 2 – ADME (Absorption, Distribution, Metabolism and Excretion): basics
Part 3 – Acute systemic toxicity (oral, dermal, inhalation)
Part 4 – Local tolerance: dermal and ocular
Part 5 – Skin sensitisation
Part 6 – Repeated-dose and chronic toxicity
Part 7 – Reproductive toxicity and teratogenicity
Part 8 – Mutagenesis and genotoxicity
Part 9 – Carcinogenicity
Part 10 – Introduction to non-experimental alternative methods used in toxicology
Part 11 – Introduction to the determination of Toxicity Reference Values
Part 12 – Introduction to human health Risk Assessment
Part 13 – Toxicology as described in a regulatory dossier (REACH) – Case study

2 days

2 200 Excl VAT

Objectives

In the context of product safety:

►  Understand  the place of toxicology in the life of substances according to the regulations

►  Know the main tests, the difficulties and issues implied

►  Optimize the interactions between Managers and Experts

Target

► Product safety departments

Fiche pdf

Trainers

Carole CHARMEAU - GENEVOIS
Expert Toxicologist
more detailsCarole Charmeau holds a PhD in Toxicology and is qualified as a European Registered Toxicologist (ERT). She has 20 years of experience with industrial chemicals and agrochemicals gained at IARC and Rhodia. She joined CEHTRA in 2008 as a senior toxicologist to strengthen the REACH team, providing strategy to assess the hazard of chemicals for human health using alternative methods. Carole is also specialised in the derivation of Derived No Effect Levels for the human. She developped the IFRA consumer exposure scenarios guidance (2011) and was involved in ECHA’s project for the consumer risk assessment developing scenarios in ConsExpo to be imported in CHESAR. Since 2014, Carole has participated in human health R&D projects at KREATiS, a daughter company of CEHTRA specialised in the development of High Accuracy In-Silico models to predict regulatory experimental endpoints such as skin/eye irritation potential or skin sensitisation potential of chemicals. In January 2018, Carole joined KREATiS as Managing Director of the company where she continues to provide expert toxicology advice for both CEHTRA and KREATiS.
Marie-Charlotte BERNIER
Toxicologist
more detailsMarie-Charlotte BERNIER holds a PhD in Toxicology of nanomaterials and a Master in Toxicology. She is qualified as a European Registered Toxicologists (ERT) since 2017. Marie-Charlotte joined CEHTRA in 2012 as a toxicologist/safety assessor for cosmetics (cosmetic safety report; evaluation of the safety of raw materials and packaging). She now provides her expertise for REACH dossiers in tasks related to the assessment of human health hazard (data evaluation, datagap analysis, study monitoring, classification, DNELs calculation, etc). She is also involved in regulatory dossiers such as Food/Food contact. More recently, she acquired new responsibilities for Medical Devices division and the Biological Evaluation of MDs. She also provides training in Regulatory toxicology and risk assessment.
  • BIOCIDES
  • CHEMICALS
  • REACH AUTHORISATION
  • COSMETICS
  • FOOD & PACKAGING
  • PHARMACEUTICALS
  • PLANT PROTECTION
  • MEDICAL DEVICES
  • Home
  • Our DNA
  • Contact us
  • Outsourcing
  • Meet the experts
  • Posters
  • CEHTRA near you
  • Job offers
  • News & Events
  • Legal
  • Data privacy
Cehtra LinkedinCehtra Twitter

®CEHTRA