Buy or sell a verified pharma plant in India.
GMP, WHO-GMP, and Schedule M compliant manufacturing units — every listing pre-screened for licences, documentation, and site condition. NDA-first, end to end, from inquiry to handover.
Every plant is screened before it's listed.
Backed by 23+ years in pharmaceutical QA, QC, and regulatory affairs — we check what a buyer's due-diligence team would check, before you ever see the listing.
Licence & Certification
Drug manufacturing licences, GMP / WHO-GMP certificates, and section-wise approvals are verified against the originals — including validity dates.
Documentation Audit
Land and building ownership, pollution control NOC, machinery records, and pending litigation status reviewed for a clean, transferable deal.
Site Condition Review
Facility layout, utilities, and Revised Schedule M readiness assessed so you know upgrade costs before negotiation — not after possession.
Pharma plants across India.
Filter by what matters to you — every card links to the complete dossier with licence numbers, machinery lists, and section approvals.
WHO-Certified Running Pharma Plant — Tablet, Capsule & Liquid Unit
GMP Pharma Plant — Tablets, Liquids & External Preparations Unit
Revised Schedule M Compliant Unit for Rent — Fast Manufacturing Entry
No listed plant matches those filters right now — but new verified listings are added regularly, and unlisted opportunities exist off-market.
Tell Us Your Requirement on WhatsAppSimple, transparent, confidential.
From first inquiry to regulatory handover — one team, one accountable process.
Submit Your Interest
Buyer or seller shares basic details through the secure form or WhatsApp. Quick, confidential, and commitment-free.
Verification & Shortlisting
We verify documentation, licences, and site condition — then match verified buyers with verified sellers under NDA.
Deal Coordination
Site visits, negotiation support, and complete regulatory handover — licence transfer guidance included, through to possession.
List your plant confidentially.
Your identity and plant details are never published without written consent. Serious, verified buyers only.
Before you buy or sell.
What exactly is verified before a plant is listed?
Drug manufacturing licences with section-wise approvals, GMP or WHO-GMP certificates and their validity, land and building ownership documents, pollution control consent, and the machinery record. Site condition and Revised Schedule M readiness are assessed separately so buyers know upgrade costs upfront.
Is my inquiry confidential?
Yes. Seller identity and plant details are never published without written consent, and buyer requirements are shared with sellers only after intent verification. An NDA is available before any document changes hands.
Why does Revised Schedule M matter when buying a plant?
Revised Schedule M (2023) raised the mandatory GMP baseline for Indian manufacturing units — covering premises, HVAC, water systems, and documentation. A plant that isn't compliant may need significant upgrade investment after purchase, which is why compliance status is assessed and disclosed on every listing.
Can I buy a plant in a state where I don't hold a drug licence?
Yes — manufacturing licences are premises-linked and state-issued, so the transaction typically involves either transfer formalities or a fresh application with the state licensing authority. We guide both routes as part of deal coordination, including the regulatory handover.
What happens after I shortlist a plant?
We arrange the site visit, put the NDA in place, support negotiation, and coordinate the regulatory and documentation handover through to possession — one accountable team across the whole transaction.
Ready to buy or sell a pharma plant?
Tell us your requirement — plant, sections, state, budget — and get matched confidentially.