About
A Decade in Pharmaceutical Sourcing
NK Industries is a pharmaceutical sourcing, supply, and manufacturing consultancy based in Maharashtra, India. We connect pharmaceutical manufacturers, CROs, CDMOs, and research organisations with qualified material sources across India and internationally.
What NK Industries Does
NK Industries is not a manufacturer. We are a sourcing, supply, and coordination business that sits between the buyer (a pharmaceutical manufacturer, CRO, CDMO, or research organisation) and the manufacturing base.
Our work covers six product categories: API intermediates and key starting materials, precious metal catalysts, impurity reference standards, pharma-grade solvents, specialty and fine chemicals, and custom synthesis services (CRAMS). Within each category, we manage sourcing, analytical verification, documentation packaging, and logistics.
For buyers who need a single material or a single batch, we function as a responsive vendor. For buyers who need a standing supply of multiple materials, we set up a structured supply framework with pre-agreed specifications, pricing, and lead times.
Therapeutic Focus
Our primary therapeutic areas are oncology and antidiabetic. These account for the largest share of our intermediate and catalyst supply. We are expanding into cardiovascular, CNS, and anti-infective as enquiry volumes in those areas grow.
Our Manufacturing Network
We work with 50+ qualified manufacturers and suppliers across the four primary pharmaceutical manufacturing states in India. Our network includes cGMP API facilities, fine chemical manufacturers, analytical reference standard producers, and specialty chemical suppliers.
For materials not available domestically, we import through our active IEC (BPLPK4014D). Export of certified materials to international buyers is an active part of our business and is growing.
Regulatory Posture
NK Industries does not hold its own manufacturing certification. We are a sourcing and supply consultancy. Regulated supply is provided through qualified cGMP partner facilities with full batch documentation. Our documentation standard is FDA-referenced: COA with full spectral pack, MSDS, and regulatory declarations formatted for ICH Q3A/B and ICH Q7 filing.
Registration and Compliance
Registered Address
04 Punyai Complex
Golegaon Road, Shirur
Pune 412210
Maharashtra, India
Work With Us
Whether you are a procurement manager at a pharmaceutical company, a consultant sourcing for multiple clients, or an export house looking for a reliable Indian supplier, we are structured to work with you.
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