Safety Pharmacology Services
An integrated approach to GLP and Non-GLP Safety Pharmacology assessments to help you progress from Discovery through ICH.
Comply, lower risk and add value to your molecule.
You need to meet the regulatory requirements of the ICH core battery studies. But, what about your own business risks? With many compounds, it’s possible to clear ICH hurdles only to face a host of safety endpoint issues as you advance from discovery, through early development and into clinical study phases. You need a value-added partner to help identify unsafe compounds earlier than ever before, at the lowest possible cost.
Know more, earlier than ever before.
By looking at safety pharmacology through a business risk lens, you begin to see the process of safety assessment in an entirely different light. We call it VAST — Value Added Safety pharmacology & Toxicology. Now you can economically assess your safety pharmacology endpoints during your toxicology studies to make better safety predictions, earlier than ever before. With many compounds running into safety issues during the clinical phases, there is a great opportunity to anticipate these data in your nonclinical stage, saving you time and money long-term. By better understanding and reducing the risk of drug attrition of your molecule, you are able to progress forward with more confidence — and with the right molecules. Rethink what’s possible and gain a markedly different approach to your early safety assessment regimen.
A suite of services, all integrated for earlier insights.
We offer you an integrated approach to non-GLP and GLP Safety Pharmacology assessment to help you progress from Discovery through ICH.
Our multi-disciplinary team is well positioned to help you obtain your safety pharmacology endpoints to meet regulatory requirements, uncover future issues and advance the best molecules.
We partner with you to provide: