18Objectives: Our objective was to review the literature on the inferred duration of the infectious 19 period of COVID-19, caused by SARS-COV-2 virus, and provide an overview of the variation 20 depending on the methodological approach. 21 Design: Rapid scoping review. Literature review with fixed search terms, up to 1 st April 2020. Central 22 tendency and variation of the parameter estimates for infectious period in (a) asymptomatic (b) 23 symptomatic cases from (i) virological studies (repeated testing), (ii) tracing studies (iii) modelling 24 studies were gathered. Narrative review of viral dynamics. 25 Information sources: Search strategies developed and the following searched: PubMed, Google 26 Scholar, MedRxiv, BioRxiv. Additionally, the Health Information Quality Authority (Ireland) viral load 27 synthesis was utilised, which screened literature from PubMed, Embase, ScienceDirect, NHS 28 evidence, Cochrane, medRxiv and bioRxiv, HRB open databases. 29Results: There was substantial variation in the estimates, and how infectious period was inferred. 30One study provided approximate median infectious period for asymptomatic cases of 6.5-9.5 days. 31Median pre-symptomatic infectious period across studies varied over <1-4 days. Estimated mean 32 time from symptom onset to two negative RT-PCR tests was 13.4 days (95%CI: 10.9-15.8), but was 33 shorter when studies included children or less severe cases. Estimated mean duration from 34 symptom onset to hospital discharge or death (potential maximal infectious period) was 18.1 days 35 (95%CI: 15.1-21.0); time to discharge was on average 4 days shorter than time-to-death. Viral 36 dynamic data and model infectious parameters were often shorter than repeated diagnostic data. 37Conclusions: There are limitations of inferring infectiousness from repeated diagnosis, viral loads, 38 and viral replication data alone, and also potential patient recall bias relevant to estimating exposure 39 and symptom onset times. Despite this, available data provides a preliminary evidence base to 40 inform models of central tendency for key parameters, and variation for exploring parameter space 41 and sensitivity analysis. Some current models may be underestimating infectious period. 42 . CC-BY 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. (which was not certified by peer review)