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Product Registration and Regulatory Compliance
REACH Regulation
UK REACH
PBT and vPvB Assessments
Classification Labelling and Packaging (CLP) Regulation
Evaluation of Endocrine Disrupting Properties
Pharmaceutical Environmental Risk and Impact Assessments
Veterinary Medicine Environmental Risk and Impact Assessment
Regulatory advice and training
Biocidal Products Regulation
Chemical Hazard and Risk Assessment
Environmental Quality Standards (EQS) Derivation and Implementation
Waste Management Consulting and Risk Assessment
Toxicology and Human Health Risk Assessment
Human Health Risk Assessment
Mode and Mechanism of Action
Toxicity Profiles
Study Design, Monitoring and Interpretation
PDE assessments
Modelling Analysis
Bioavailability of Metals
Chemical Exposure Assessment and Modelling
Supply and Value Chain / Chemical Impact Assessment
Socio-economic Analysis (SEA) of Chemicals Legislation
EU Ecolabel Application Assistance
Environmental and Regulatory Foresight
From the blog
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Clarification on some aspects of the European Medicine Agency’s revised ERA guidance
The European Medicines Agency (EMA) held a webinar on the revised guideline for the environmental risk assessment (ERA) of human pharmaceuticals in October 2025, and a summary…
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