Prosper Gold Corp. has completed Phase 1 of the drill program at the Ashley Gold Project in Northern Ontario. Phase 1 consisted of 23 drill holes for a total of 8,715 metres. Phase 2 of the drill program is targeting new syenite and structurally controlled gold targets immediately northwest and northeast of the Young Davidson (Alamos Gold) Mine property and will commence in March 2017. Drilling to date has targeted the Ashley-Garvey vein system near the historic Ashley Gold Mine. Drilling tested the hangingwall, footwall, down-dip and northward and southward on-strike continuity of the Ashley and Garvey veins and newly discovered gold-in-soil anomalies. A substantial quartz feldspar porphyry-quartz syenite discovered west of the vein systems requires further drill testing. Prosper Gold has applied a rigorous quality assurance/quality control program at the Ashley Project using industry best practice. The core is logged, recovery and rock quality designation calculated, fractures counted and magnetic susceptibility measured. Orientation of fractures, veins and contacts are measured (oriented core is used). Drill core is sawn in half lengthwise at the core logging facility in Matachewan and sampled in one and two metre intervals. Half of the core is placed in plastic bags and sealed and the remaining half core is retained in core boxes stored at the project. The program includes chain of custody of samples from drill to laboratory. A standard sample, a blank sample, or a duplicate sample is inserted into the sample stream every tenth sample. Three certified ore assay laboratory standards used in the process, were supplied by CDN Resource Laboratories Ltd. In total, 397 quality control samples (about 11% of 3,740 samples) were analyzed. As well 292 assay pulps retained at the Timmins ALS preparation lab are being reanalyzed by gold fire assay at Actlabs in Timmins as a double check on initial gold results. A further 184 samples were analyzed by metallic screen analysis at Actlabs in Ancaster Ontario. A representative 1000-gram split is sieved at 100 mesh (149 micron) with assays of the entire +100-mesh and on 2 splits of the -100-mesh fraction. The final assay is calculated based on the weight of each fraction.