<p data-start="225" data-end="766">The Revised Schedule M in Pharmacy Guidelines introduces upgraded Good Manufacturing Practices (GMP) for pharmaceutical units in India. These changes focus on enhanced quality control, improved facility standards, upgraded documentation processes, and stricter validation protocols. Manufacturers must comply with the revised norms to continue operations and ensure product consistency. Agile Regulatory provides expert support to help pharma companies understand the new requirements and implement the updated Schedule M standards smoothly.