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.
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Study following the specifications validated with the Expert.
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