Schedule M regulations define the mandatory GMP framework for drug manufacturers. This overview explains schedule M guidelines, their legal scope, and practical impact on facility design, documentation, and quality systems. It clarifies how Schedule M in pharma ensures product safety, consistency, and compliance, and why Schedule M in pharmacy operations is critical for licensing, inspections, and sustained regulatory approval requirements across manufacturing units.

Learn more: https://pd-vd.com/what-are-schedule-m-guidelines/