Competitive PCR is an efficient way for the measurement of nucleic acids without requiring a standard curve. It uses a competitor template mimicking the target sequence for direct comparison and quantification during amplification. However, manually preparing various concentrations for competitive PCR is labor-intensive. Additionally, target and competitor DNA bands are often inadequately separated on gels due to their similar sizes. This leads to inaccurate distinction and imprecise measurement of bandwidths and intensities, resulting in high standard deviations in quantification. Thus, this study presents an alternative way to combine droplet competitive PCR with the concentration gradient generator in a microfluidic device that simplifies competitive PCR preparation and provides precise control over reaction conditions and sample handling. Generating a wide range of competitor-to-target ratios in a single experiment enhances statistical reliability and isolating individual reactions in droplets reduces background noise and increases sensitivity. Additionally, it eliminates gel electrophoresis, improves consistency and reproducibility, requires smaller sample and reagent volumes, and allows direct sample quantification through a calibration curve for fast, simple quantification. We envision that our platform can offer a promising alternative to digital PCR, addressing its challenges and driving progress in molecular biology and diagnostics.