Coronavirus disease 2019 (COVID-19) is a transmitted respiratory disease caused by the
infection of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although
humankind has experienced several outbreaks of infectious diseases, the COVID-19
pandemic has the highest rate of infection and has had high levels of social and
economic repercussions. The current COVID-19 pandemic has highlighted the limitations of
existing virological tests, which have failed to be adopted at a rate to properly slow
the rapid spread of SARS-CoV-2. Pandemic preparedness has developed as a focus of many
governments around the world in the event of a future outbreak. Despite the largely
widespread availability of vaccines, the importance of testing has not diminished to
monitor the evolution of the virus and the resulting stages of the pandemic. Therefore,
developing diagnostic technology that serves as a line of defense has become imperative.
In particular, that test should satisfy three criteria to be widely adopted: simplicity,
economic feasibility, and accessibility. At the heart of it all, it must enable early
diagnosis in the course of infection to reduce spread. However, diagnostic manufacturers
need guidance on the optimal characteristics of a virological test to ensure pandemic
preparedness and to aid in the effective treatment of viral infections. Nanomaterials
are a decisive element in developing COVID-19 diagnostic kits as well as a key
contributor to enhance the performance of existing tests. Our objective is to develop a
profile of the criteria that should be available in a platform as the target product. In
this work, virus detection tests were evaluated from the perspective of the COVID-19
pandemic, and then we generalized the requirements to develop a target product profile
for a platform for virus detection.