For any product manufacturer or developer in the nicotine, pharmaceutical or medicinal cannabis industry, it’s essential that you have robust reliable toxicological data.
Toxicology assessments can be time consuming; but, it’s an area wherein product developers can reduce lead times and bring products to market quicker.
Here, Dean Hatt, Senior Toxicology Consultant and Toxicology Manager at contract research organisation, Broughton, explains how digital repositories and tools can aid the process.
The process of bringing a new drug to market in the UK is extensive and typically spans several years. This timeline encompasses drug discovery, preclinical studies, including toxicology profiling, clinical trials and regulatory approval.
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