Safety pharmacology studies are needed for assessment of the impact of any new chemical entity or biotechnology-derived product on vital organ systems before first-in-human drug testing. These evaluations are essential steps in assessing of any acute or potentially life-threatening risks for the novel pharmaceuticals. Understanding of drug’s impact on vital organ systems helps the planning for all of the following human trials. Aurora’s safety pharmacology services help the researchers for getting data that meets all regulatory standards and used for an smooth transition of preclinical to clinical pharmacology. Our experts conduct safety pharmacology studies for your new chemical entity or biotechnology-derived product according to ICH safety pharmacology guidance.
Aurora Contract Research Services, using label free technology and various animal models helps to make your drug discovery experimental design and data interpretation fast and easy. Contact us for a more in-depth discussion on how our provided assays can be customized to meet your specific goals.