India supplies medicines to much of the world, and that position depends on manufacturing quality that can survive scrutiny from regulators and buyers on every continent. A single undetected equipment defect or facility gap doesn’t just risk a batch — it risks a regulator’s confidence in the entire plant.
TNV Inspection Division provides UAF-accredited third party inspection services for pharmaceutical equipment and facilities across India, under ISO/IEC 17020:2012 (Accreditation No. 5241222IB04). As a Type A inspection body, we hold no commercial stake in the manufacturer, equipment supplier, or EPC contractor. Our inspectors verify materials, fabrication, and installation against the applicable technical specifications.
We work with pharmaceutical manufacturers, equipment suppliers, and EPC contractors building or upgrading facilities across India’s pharma sector.
Verify our accreditation at any time: certificate.tnvib.com
What is Pharmaceutical Inspection?
Pharmaceutical inspection is the independent verification of manufacturing equipment, facility systems, and process infrastructure against applicable technical specifications and regulatory expectations, including Schedule M requirements under the Drugs and Cosmetics Rules.
It is distinct from a GMP audit or certification inspection focuses on verifying that specific equipment and infrastructure meet what was specified, covering:
- Process equipment inspection verifying reactors, mixers, tablet compression machines, and other manufacturing equipment against purchase specifications
- HVAC and clean utility system inspection checking air handling units, clean room systems, and water-for-injection systems against design specifications
- Storage and cold-chain infrastructure inspection verifying cold storage, warehousing, and temperature-controlled logistics equipment
- Packaging line inspection checking packaging and labelling equipment for conformance to specification
- Civil and structural inspection verifying facility construction elements relevant to manufacturing compliance, such as flooring, wall finishes, and utility routing
- Factory inspection before dispatch verifying equipment at the manufacturer’s facility before it is shipped and installed
Why Pharmaceutical Inspection Matters in India
- India’s Pharma Sector Carries Global Responsibility As one of the world’s largest suppliers of generic medicines and vaccines, India’s pharmaceutical manufacturing quality is scrutinised by regulators and buyers across multiple countries. Independent, documented verification of equipment and facilities supports that scrutiny rather than leaving it entirely to internal claims.
- Schedule M Sets a Rising Compliance Bar Schedule M under the Drugs and Cosmetics Rules sets manufacturing infrastructure and quality system requirements for Indian pharma facilities, and recent revisions have raised expectations further, particularly for smaller manufacturers. Independent inspection helps manufacturers verify that equipment and facility elements genuinely meet what the specification calls for.
- Equipment Defects Are Costly to Catch Late A process equipment fault or a clean utility system gap that goes undetected during installation can affect product quality long after the facility is operational, and is far more expensive and disruptive to correct once production has begun.
- Manufacturers Need a Documented, Independent Record Whether preparing for a regulatory inspection, a buyer audit, or an internal quality review, manufacturers benefit from an independent, dated record showing that equipment and facility elements were verified against specification — something internal engineering sign-off alone does not carry the same weight for.
Pharmaceutical Inspection Services by TNV
- Process Equipment Inspection Inspection of manufacturing equipment such as reactors, mixers, granulators, and tablet compression machines, verified against the purchase specification and factory test results.
- HVAC and Clean Utility System Inspection Verification of air handling units, clean room systems, and water systems against the design specification, relevant to maintaining controlled manufacturing environments.
- Storage and Cold-Chain Infrastructure Inspection Inspection of cold storage, warehousing, and temperature-controlled logistics equipment used in pharmaceutical storage and distribution.
- Packaging Line Inspection Verification of packaging and labelling equipment for conformance to specification and operational requirements.
- Facility Construction and Civil Inspection Inspection of civil and structural elements relevant to manufacturing compliance during facility construction or upgrade.
- Factory Inspection Before Dispatch Inspection of pharmaceutical process equipment at the manufacturer’s facility before it is shipped, verifying materials, fabrication quality, and factory test results.
Where We Provide Pharmaceutical Inspection Services
TNV provides pharmaceutical inspection services across India’s major pharma manufacturing clusters, with strong active coverage in:
- Telangana pharma manufacturing and bulk drug clusters around Hyderabad
- Gujarat pharmaceutical facilities across Ahmedabad and surrounding industrial belts
- Maharashtra pharma manufacturing around Mumbai and Pune
- Uttar Pradesh pharma and allied manufacturing projects, supported by our Lucknow head office
For projects in other pharma manufacturing hubs, contact us directly we mobilise inspectors across India for pharmaceutical assignments.
How Our Pharmaceutical Inspection Works
- Step 1 — Scope and Specification Confirmation You share equipment drawings, facility specifications, and applicable Schedule M or design requirements. We confirm scope and provide a cost estimate.
- Step 2 — Inspector Assignment We assign inspectors experienced in pharmaceutical equipment and facility inspection.
- Step 3 — Equipment or Facility Inspection Our inspectors verify equipment, systems, or civil elements against the specification, at the manufacturer’s facility or the project site as required.
- Step 4 — Inspection Reports You receive a detailed report covering findings, photographic evidence, and any non-conformances identified against the specification.
- Step 5 — Follow-Up and Closeout Verification Where non-conformances are found, we support corrective action verification and re-inspection before sign-off.
Why TNV Is the Right Choice for Pharmaceutical Inspection in India
- UAF Accreditation — Internationally Recognised TNV Global Limited is accredited by the United Accreditation Foundation (UAF), an IAF MLA signatory and APAC MRA signatory. Accreditation No. 5241222IB04, valid through December 2028.
- Type A Independence TNV has no financial relationship with pharmaceutical manufacturers, equipment suppliers, or EPC contractors in this sector. Our findings are not shaped by commercial pressure from any party.
- Experience Across Equipment and Facility Types Our inspectors cover process equipment, clean utility systems, storage infrastructure, and civil construction, giving pharma manufacturers a single, consistent inspection partner.
- Coverage Across Manufacturing Clusters We are structured to inspect across India’s major pharma hubs, which suits manufacturers and EPC contractors managing multiple facility or equipment projects at once.
- Trusted by Established Indian Organisations Our client base includes IRCTC, Adani Wilmar, Patanjali Ayurved, and ICAR, reflecting a track record across regulated, safety-conscious Indian sectors.
- Verifiable Accreditation Our accreditation status can be verified at any time at certificate.tnvib.com.
Contact Us for a Pharmaceutical Inspection Quote in India
Tell us about your equipment, facility, or process system and applicable specifications. We will respond within one business day with a scope confirmation and cost estimate.
Email: info@tnvib.com
Website: www.tnvib.com
Head Office: TNV House, B-1/19/69, Sector-K, Aliganj, Lucknow, Uttar Pradesh 226204, India
Frequently Asked Questions About Pharmaceutical Inspection
Does TNV certify pharmaceutical facilities for GMP compliance?
No. TNV is an inspection body, not a certification body. We independently inspect and verify pharmaceutical equipment, facilities, and process systems against applicable specifications and Schedule M requirements. GMP certification itself is issued by the relevant drug regulatory authority, not by TNV.
What does TNV inspect at pharmaceutical facilities?
TNV inspects process equipment such as reactors, mixers, and tablet compression machines, HVAC and clean utility systems, storage and cold-chain infrastructure, packaging line equipment, and civil and structural elements of manufacturing facilities against applicable specifications and Schedule M requirements.
Can TNV inspect equipment before it is installed at a pharma facility?
Yes. TNV carries out factory inspection of pharmaceutical process equipment before dispatch, verifying materials, fabrication quality, and factory test results against the purchase order and applicable specifications.
How much does pharmaceutical inspection cost in India?
Cost depends on the scope of equipment or facility being inspected, location, and testing requirements. Contact us at info@tnvib.com for a specific quote initial enquiries are free.
Is TNV's inspection recognised for Schedule M or WHO-GMP compliance purposes?
TNV is a UAF-accredited Type A inspection body under ISO/IEC 17020:2012, and our reports document independent, standards-based inspection findings that manufacturers can use to demonstrate due diligence as part of their Schedule M or WHO-GMP compliance efforts. Manufacturers should confirm specific documentation requirements with the relevant drug regulatory authority or their compliance advisor for their particular facility.