Meeting the requirements of FDA/NMPA/EMA
One-time IND approval
Toxicology is an important part of drug development, which explore the damage of drugs to the body under certain conditions. It is forced to carry out before First in human Clinical trials by agencies, and play a critical role in risk identification and control in clinical. Genscript Probio integrated high-quality resources to provide a variety of Preclinical studies for IND filling, including efficacy, PK studies and toxicology study (Non-GLP & GLP).
IND filling Package
Please download service quotation form and fill it before sending to us.