Reviews post-marketing requirement (PMR) and post-marketing commitment (PMC) wording, study designs, and timetables for clinical pharmacology content — verifying that each commitment is scientifically feasible as worded, that the proposed design answers the stated question, and that timetables are internally consistent. Use when reviewing draft PMR/PMC language before agreement with an agency. Do not use for PMR/PMC execution tracking, for post-approval change impact, or for deciding what to commit to.
