About Naprod
Sovereign in Oncology. Sovereign in Operation.
Naprod Life Sciences Pvt. Ltd. has manufactured oncology, anesthesia, and critical-care injectables at a single site in Tarapur, Maharashtra, since 1994 — one plant, one quality system, three decades of continuous production.
163 products across FDF and API tiers, spanning SRA/EU export, ROW export, and domestic markets.
1994 to today
Three decades at one address
Every milestone below is a named, dated event at the Tarapur facility — the 2026 ANVISA renewal is independently confirmed by third-party reporting; earlier dates are drawn from an internal draft and flagged pending confirmation.
- 1994
Naprod founded
Naprod Life Sciences began production of oncology, anesthesia, and critical-care injectables at Boisar, Maharashtra (company later incorporated in 2006).
- 2009
Lyophilization capability added
Added lyophilized injectable manufacturing capability at the Tarapur facility, expanding beyond liquid formulations.
- 2013
WHO-GMP certification
Received WHO-GMP certification for the Tarapur facility, opening pathways into regulatory frameworks that reference WHO-GMP-listed manufacturers.
- 2016
Latin America market entry
Entered Latin American markets following ANVISA (Brazil) and INVIMA (Colombia) regulatory approvals.
- 2020
EU-GMP certification
Achieved EU-GMP certification for the Tarapur facility, enabling direct supply into European Economic Area markets.
- 2026
ANVISA GMP renewal
ANVISA renewed the Tarapur plant's GMP certification in January 2026, reaffirming continuous Brazilian market access.
What guides the work
Seven operating values
These placeholder values describe the operating disciplines behind Naprod's manufacturing and quality decisions. Naprod's live-site values are authoritative and were not recoverable from available source material — this set must be replaced before publishing.
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Quality Without Compromise
Every batch is manufactured and released against documented GMP standards, with no shortcuts on testing or release criteria.
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Regulatory Integrity
Filings, dossiers, and inspection findings are handled with complete transparency toward regulators and customers.
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Reliability of Supply
Capacity planning and shift scheduling are structured to protect continuity of supply for partner markets.
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Scientific Rigor
Formulation and process decisions are grounded in validated data, not assumption.
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People First
Manufacturing and quality outcomes depend on trained, accountable teams at every shift and station.
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Continuous Improvement
Processes, yields, and documentation are reviewed on a standing cadence rather than only after a deviation.
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Responsible Operations
Environmental, health, and safety practices at the Tarapur site are treated as a standing operating requirement, not an add-on.
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Who we are
A manufacturer, not an intermediary
Naprod Life Sciences Pvt. Ltd. is a manufacturer of sterile and non-sterile pharmaceutical products, built around three therapeutic lines: oncology, anesthesia, and critical-care injectables. Manufacturing is consolidated at a single site — MIDC Tarapur, Boisar, Maharashtra, India (DUNS 915076185) — where lyophilized injectables, liquid injectables, tablets, and capsules are formulated, filled, and released under one quality system. Naprod also carries a dedicated Contract Development and Manufacturing Organization (CDMO) capability for partners who need process development and manufacturing scale on top of the existing plant infrastructure — a service built on the same regulatory base as the branded catalog, not a separate business.
1994 to today
Three decades at one address
Naprod began production of oncology, anesthesia, and critical-care injectables at Boisar, Maharashtra in 1994; the company was formally incorporated in 2006. Lyophilization capability was added at the Tarapur facility to extend beyond liquid formulations, and the plant subsequently earned WHO-GMP certification, opening pathways into regulatory frameworks that reference WHO-GMP-listed manufacturers. Latin American market entry followed direct ANVISA (Brazil) and INVIMA (Colombia) regulatory approvals, and EU-GMP certification later enabled direct supply into European Economic Area markets. Most recently, ANVISA renewed the Tarapur plant's GMP certification in January 2026, reaffirming continuous Brazilian market access — reported by Pharma India Magazine.
Pending approval Dates between the 1994 founding and the January 2026 ANVISA renewal are sourced from an internal IT-team draft and are pending confirmation against company records.
Manufacturing base
One site, four dosage families
The Tarapur facility runs six declared production lines: oncology lyophilized injectables, oncology liquid injectables, tablets, capsules, general lyophilized injectables, and general liquid injectables. The current catalog spans 163 products — 100 finished dosage form (FDF) and 63 active pharmaceutical ingredient (API) — sold across SRA/EU export, rest-of-world (ROW) export, and domestic tiers. API supply is produced by MacChem, presented here as a group company.
Pending approval Annual capacity figures (oncology lyophilized 3.5M units, oncology liquid 3M, tablets 30M, capsules 15M, general lyophilized 10M, general liquid 1M) are carried over from a company draft and are pending confirmation.
Regulatory standing
Six accreditations independently verified
Naprod's Tarapur facility holds direct plant-level accreditation from EU-GMP, ANVISA (Brazil), INVIMA (Colombia), the UAE Ministry of Health and Prevention, Bahrain's National Health Regulatory Authority, and WHO-GMP — each confirmed against an official regulator source. A further slate of national agency relationships across Latin America, Africa, Southeast Asia, CIS/Ukraine, and South Asia is on record internally and is being digitized toward a target register of roughly 21 accreditations.
Pending approval Beyond the six independently verified accreditations, the wider ~21-agency register is an internal draft awaiting company sign-off before publication as verified.
Leadership
Director-led, plant-based oversight
Mohan B. Jain serves as Director of Naprod Life Sciences Pvt. Ltd., overseeing the Tarapur manufacturing base. He is currently the only Naprod leader approved for public identification on this site.
Pending approval The wider leadership team (CEO, COO, Head of Quality Assurance, Head of Manufacturing Operations, Head of R&D) is PENDING APPROVAL and withheld from public identification until the company confirms names and titles.
What guides the work
Seven operating values
Naprod orients daily manufacturing and quality decisions around seven standing values: quality without compromise, regulatory integrity, reliability of supply, scientific rigor, people first, continuous improvement, and responsible operations. Each value maps to a concrete operating discipline — documented GMP release criteria, transparent regulator and customer communication, capacity planning for supply continuity, validated-data-driven process decisions, trained and accountable shift teams, a standing review cadence rather than deviation-only reviews, and environmental/health/safety practice treated as a standing requirement at the Tarapur site.
Pending approval The seven values listed are placeholders pending confirmation — Naprod's live-site values are authoritative and were not recoverable from available source material; this set must be replaced with the company-confirmed list before publishing.