This CMS-approved gynecologic cytopathology proficiency testing program is designed according to federal CLIA regulations to test basic diagnostic skills for gynecologic cytopathology specimens. It leverages the experience gained from 19,000 individual tests, as well as the collective knowledge of cytopathology experts serving on the ASCP GYN PT™ & Assessment Committee.

Choose the date you want to conduct your testing and the type of materials you want to use. All results are returned within 15 business days or less from the date the testing materials are received by ASCP. The referee panel includes three physicians and two cytotechnologists.

These activities meet MOC Part II Lifelong Learning requirements. These activities meet MOC Part IV Quality Assurance requirements.