Welcome to Nirmay Pharma Pvt. Ltd. ☎ +91-361-2XXXXXX  |  ✉ info@nirmaypharma.com
Committed to Quality, Dedicated to Health WHO-GMP Certified · ISO 9001:2015 · Established 2003

Manufacturing & Quality

Two units. One campus. One quality standard. Both of our WHO-GMP certified facilities are located at the Brahmaputra Industrial Park in Amingaon, Guwahati — on adjacent plots within the same industrial estate.

Combined built-up area Installed capacity Production assets
~22,000 sq.m. 700 million units / year ~140 equipment

Unit 1 — Amingaon (Oral Solid Dosage)

Our primary oral solid dosage facility — tablets, film-coated tablets, and hard-gelatin capsules — with a segregated beta-lactam block operated under independent HVAC and effluent systems.

Address
Plot 12, Brahmaputra Industrial Park, Amingaon, Guwahati – 781031
Commissioned
2005
Built-up area
~13,500 sq.m.
Primary dosage forms
Tablets, film-coated tablets, hard-gelatin capsules
Annual capacity
500M tablets · 150M capsules
Segregated blocks
Beta-lactam wing (independent HVAC and effluent)
Certifications
WHO-GMP · ISO 9001:2015 · ISO 14001:2015

Unit 2 — Amingaon (Liquid Orals & Semi-solids)

Adjacent to Unit 1 on the same industrial park, this facility handles liquid oral formulations — syrups, dry syrups, suspensions — and non-sterile semi-solid preparations such as ointments and creams.

Address
Plot 14, Brahmaputra Industrial Park, Amingaon, Guwahati – 781031
Commissioned
2011
Built-up area
~8,500 sq.m.
Primary dosage forms
Syrups, dry syrups, oral suspensions, ointments, creams
Annual capacity
42M bottles (pooled) · 6M tubes (semi-solids)
Line count
2 liquid fill lines · 1 dry-syrup line · 1 semi-solid line
Certifications
WHO-GMP · ISO 9001:2015

Quality Systems

Both units operate under a unified Quality Management System aligned with WHO-GMP, ICH Q7/Q9/Q10 guidance, and ISO 9001:2015. Each batch is released under the signature of a Qualified Person following in-process and finished-product testing against pharmacopoeial specifications.

Area Summary
QA / QC laboratories Shared analytical laboratory serving both units, equipped with HPLC systems, dissolution apparatus, Karl Fischer titrators, FT-IR, UV-visible spectrophotometers, and walk-in stability chambers under ICH Q1A conditions.
Calibration & qualification A central calibration master plan covers ~140 production and laboratory instruments across both units, with periodic re-qualification under our Validation Master Plan and documented change control.
Documentation & audit readiness Batch manufacturing records, deviation logs, CAPA, change control, and training records are maintained under a documented retention policy, with regular internal audits and annual management reviews.

Regulatory Approvals

Both units are regulated and inspected by the relevant national authority. Our export registrations are maintained in partnership with our country representatives.

Authority Applicability
Central Drugs Standard Control Organisation (CDSCO), IndiaBoth units
Assam State Drug ControllerBoth units
WHO-GMP (Geneva format)Unit 1 & Unit 2
Department of Drug Administration, NepalRegistered exporter
Pharmacy & Poisons Board, KenyaRegistered exporter
EFDA, EthiopiaRegistered exporter
NMRA, Sri LankaRegistered exporter
FDA, MyanmarRegistered exporter

Environment, Health & Safety

Our Amingaon campus operates a common effluent treatment plant sized for both units, with primary and secondary treatment stages before discharge into the estate-level sewer. Unit 1 has installed a 200 kWp rooftop solar array which meets approximately 28% of the campus daytime electrical demand. We are progressively transitioning to water-based coating systems in our film-coating operations and have reduced single-use plastics in our secondary packaging lines by 42% since 2021.

Our Environment, Health & Safety committee meets monthly, with a cross-unit internal audit conducted each quarter. We maintain ISO 14001:2015 certification at Unit 1, and Unit 2 is currently in the final phase of certification review.

Audit Requests & Site Visits

We welcome audits from regulatory authorities, institutional buyers, and export partners. Please contact our Business Development team to schedule a site visit or technical review.

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