Implementation of a regulatory clinical phasefor a new drug or repositioning for COVID-19: Phase I for toxicity, Phase IIa or IIb, measurement of efficacy and toxicity on a larger cohort, collection of PK/PD pharmacodynamic data.
It also applies to sample collections that require a specific protocol.
This service is designed for Biotech companies developing SARS-CoV-2 new drugs.
Materials to provide
Details about the drug development project.
Further details on the project may be requested.
You will be able to exchange directly with the experts after filling in the form below.
Typical deliverables
Study following the specifications validated with the Expert.
Get started with your COVID-19 clinical study information request
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