We're proud to receive a 2025 CDMO Leadership Award in the “Small Molecule Dosage Form - Global" category.
The pressure to file an IND makes accelerated Phase I safety testing a priority. With the Path to IND for biologics, Thermo Fisher Scientific can help deliver your large molecule drug substance for First-in-Human studies in as little as 9 months* from the start of transfection.
Now you can meet important milestones—such as filing for IND—or secure additional funding with all the confidence your project needs and, we can supply.
*Terms and Conditions: Titer levels provided are estimates based on third party results and may vary depending on molecule type or other factors. Timeline from DNA to drug product and start of clinical trials for all path to IND for biologics options may vary depending on molecule type or other factors and are estimates to be finalized after third party cell line development dates are available and confirmed. 9-month timeline will incur additional risk.