Virus titration is an important analytical method in the biopharmaceutical industry, which is widely used in the development and production of viral biological products, the validation of virus clearance and inactivation processes, and the detection of exogenous viruses to ensure the activity and effectiveness of viral biologics, as well as the viral safety of biological products. It is important to establish a fast, simple, and accurate method for the detection of virus titration. This article summarized the characteristics, principles and specific applications of the traditional, emerging and improved methods for detecting viral titer and compared their advantages and disadvantages. Some emerging methods, such as droplet digital PCR, viral quantitative capillary electrophoresis, in situ hybridization (ISH) assay with chemiluminescent detection, laser force cytology, etc., have improved the shortcomings of traditional methods such as time-consuming and labor-intensive, poor repeatability, low accuracy, and large subjectivity of results, and have achieved the advantages of rapidity, sensitivity, high degree of automation, high precision, and more robust and objective results. However, some new methods are expensive or not widely used, and it is necessary to select the appropriate virus titration method according to the experimental purpose.