Is your plant ready for a Revised Schedule M inspection?
A free self-assessment for small and medium pharma manufacturers. About 70 questions, 15–20 minutes. Every question cites the clause of Schedule M it comes from.
- Grounded in the Gazette. Built from G.S.R. 922(E), 28 December 2023 — Part I (all plants) and Part VIII (tablets & capsules).
- Private. Your answers stay in your browser. Nothing you answer is uploaded.
- A report you can use. Score by section, critical gaps first, and what to fix — printable as PDF for your management.
This is a self-assessment aid, not an inspection, certification or legal advice. It is not affiliated with CDSCO or any State Licensing Authority. Where this tool and the Gazette differ, the Gazette governs.
Answer “Yes” only if it is in place and you could show the record to an inspector today.
Self-assessed readiness
By section
Critical gaps
Critical requirements answered “No” or “Partly”. Fix these first.
Other gaps
Want help closing the record-keeping gaps?
We are building tools for small plants to run SOPs, logbooks, batch records, deviations, CAPA and change control without drowning in paper. Tell us what would help — we will reply personally.
Self-assessment generated from the answers given. Not an inspection, certification or legal advice. Source: Schedule M, G.S.R. 922(E), Ministry of Health and Family Welfare, 28 December 2023. Where this report and the Gazette differ, the Gazette governs.