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Advaita Life Sciences Pvt Ltd
About Us

Chemistry built on rigorous science.

ISOCertified Lab

Research-led chemistry, built for global pharma.

Founded in India, Advaita Life Sciences is a research-driven pharmaceutical chemistry company set up with one purpose — supplying the global pharma industry with high-quality key starting materials (KSMs), Active Pharmaceutical Ingredient (API) intermediates and impurity synthesis services, delivered on cost and on schedule.

From early-stage research through scale-up and manufacture, our work covers KSMs, API intermediates and a curated library of synthesized impurity standards. The aim is straightforward: understand what each customer actually needs, then deliver the chemistry and the data to back it up.

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Four core capabilities, one integrated lab.

API Intermediates & KSMs

End-to-end development and manufacture of the key starting materials and API intermediates that make multi-step API synthesis possible — produced under ICH Q7 GMP guidance.

Custom Synthesis

Made-to-spec, high-purity compounds engineered around your requirement — milligram research samples through ton-scale supply, with route optimisation and GMP-aligned scale-up.

Process Improvement & Tech Transfer

A complete process improvement and technology transfer service that carries your chemistry from R&D into commercial manufacturing — efficiently and inside regulatory limits.

Impurity Standards Synthesis

Targeted synthesis, isolation and purification of API impurities — process, degradation, genotoxic (GTIs), nitrosamine and metabolite reference standards, each with ICH-grade characterisation.

Analytical Characterisation

Disciplined QC using ¹H-NMR, HPLC, LC-MS and KF — every compound shipped with a complete Certificate of Analysis (CoA) attached.

Regulatory Compliance

Everything we ship is engineered to ICH guidelines — ready to slot into stability studies, method validation and impurity profiling for regulatory submissions anywhere in the world.

Where we're headed.

Our Mission

To supply the pharmaceutical industry with high-quality API intermediates, specialty chemicals and impurity synthesis services — delivered on cost and on time. We work to understand exactly what each customer needs, then meet that requirement with products and services they can rely on.

Our Vision

To grow into a globally trusted, sustainable partner in healthcare — known for high-quality, innovative and cost-effective chemistry that quietly improves lives. We get there by continuing to develop and manufacture safe, novel and affordable pharmaceuticals for the long term.

Four commitments we ship with every batch.

For us, quality isn't a certificate on the wall — it's a working set of operating rules that every chemist, every analyst and every shipment is measured against.

  • Complete characterisation — NMR, Mass, HPLC and elemental — performed on every batch.
  • Traceable paperwork — CoA, MSDS and spectra retained on file for a decade.
  • Tight confidentiality — a signed CDA is in place before any chemistry begins.
  • Closed-loop improvement — each non-conformance feeds back into a procedure update.
48 HrQuote Turnaround
GMP-AlignedQuality System
mg → kgScale Capability
ICH-GradeCharacterisation

Ready to put us to work?

From a single reference standard to a long-running custom synthesis programme — our chemists are one message away.

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