Democratizing GMP Compliance for Indian Pharma
Making the Revised Schedule M accessible, understandable, and actionable for every manufacturer, QA professional, and student in India.
The Challenge
In December 2023, the Ministry of Health and Family Welfare notified the Revised Schedule M under the Drugs and Cosmetics Act, 1945. This was a monumental shift, bringing India's Good Manufacturing Practices (GMP) in line with global standards (WHO GMP).
However, navigating hundreds of pages of legal gazette notifications is overwhelming. Understanding the exact gap between the old rules and new requirements takes hundreds of man-hours. For Micro, Small, and Medium Enterprises (MSMEs) lacking massive regulatory departments, compliance can seem insurmountable.
Our Vision
We built scheduleM.in to solve this. We believe that world-class quality should not be blocked by confusing documentation. By organizing the regulations technically and integrating advanced AI, we aim to transform the massive gazette notification into a practical, daily tool.
Why It's 100% Free
Patient safety shouldn't be hidden behind a paywall.
Every feature on this platform — the clause browser, AI chatbots, SOP analyzers, and PDF reports — is completely free for all users. We do not restrict access, we do not require credit cards, and we do not hold your data hostage. We intend to monetize in the future through B2B enterprise partnerships and custom implementations, keeping the core platform free forever for the individuals doing the hard work of compliance.
Who It's For
- ✓QA Managers & Plant Heads: Conducting gap analyses and updating QMS documentation.
- ✓Regulatory Affairs: Tracking CDSCO notifications and preparing for audits.
- ✓Drug Inspectors: Quickly referencing specific clauses against field observations.
- ✓Consultants: Using our AI tools to audit client facilities faster.
- ✓Pharmacy Students: Learning real-world GMP applications beyond the textbook.
Important Disclaimer
scheduleM.in is an independent educational and utility platform. It is not affiliated with, endorsed by, or a representative of the CDSCO, the Ministry of Health and Family Welfare, or any government entity. While we use AI to process and explain the regulations, the official Gazette Notification remains the sole legally binding document. Outputs generated by our AI tools must be verified by a qualified professional before implementation.