Our services include:
- Literature review and problem formulation
- Regulatory strategy and consultation
- Persistence, bioaccumulation and toxicity (PBT) evaluation
- Mammalian read-across and endpoint analysis
- Study design, management and analysis
- Categorical exclusion preparation
- Environmental (risk) assessment preparation
View Our Work
We carefully manage the submission of the human pharmaceutical dossier is to the United States (FDA), Europe (EMEA) and elsewhere. Waterborne Environmental is equipped to deliver a scientifically sound environmental (risk) assessment and scientific papers in peer-reviewed journals.
