Prepare summary report of initial clinical sensitivity and specificity
Prepare report on robustness of manufacturing process and assay set up. certain proprietory formulation and manufacturing process data to be kept confidential.
Analytical specificity data produced. Use potential cross reactive respiratory virus samples.
Finalise clinical validation plan with Medcaptain and IRCCS
Interim Activity Report to summarise activity by the consortia
Prepare report on diagnostic assay performance based on information to be included in the product Instructions for Use.
Searching for OpenAIRE data...