Four decades of process chemistry, built for your supply chain.
45+
15–20
8
35
7
— Why Partner With Us
A supply relationship measured in
decades, not deliverables.
Ready from day one
WHO-GMP certified and ICH Q7A compliant, with active approvals from Japan PMDA and European authorities, plus EU Written Confirmation on 35 products.
Proven at commercial volume
Three WHO-GMP certified production streams, regularly audited by leading Indian and multinational firms — not a single-line operation.
Reactions others won’t take on
Dedicated facilities for nitration, chloro-sulfonation, high-pressure oxidation, hydrogenation and more — complex synthesis kept in-house.
Backward & forward integration
We manufacture many of our own key starting materials, giving partners greater control over cost, lead time and continuity of supply.
Across the full product lifecycle
From first route scouting to full commercial-scale supply, every stage is managed under one roof and one quality system.
Stage 01
Route Scouting & Process Development
Every project starts with identifying the right synthetic pathway — balancing safety, yield, cost, and ease of scale-up. Our process chemistry team evaluates raw material security, IP considerations, and environmental impact before committing to a route.
Specialized Reaction Chemistry
Purpose-built facilities for reactions many CDMOs won’t take on in-house:
Backward & Forward Integration
We manufacture many of our own key starting materials and intermediates rather than relying solely on external suppliers — giving partners greater control over cost, lead time, and supply continuity, from pre-backward integration through forward integration stages.
Analytical & Quality Support
In-house Analytical Method Validation (AMV) and Process Validation (PV), long- and short-term stability studies, and DMF support – all conducted internally with IR, GC, HPLC, UV and Karl Fischer instrumentation, under 21 CFR Part 11 compliant QC systems.
Commercial-Scale Manufacturing
Three dedicated WHO-GMP certified production streams support everything from development quantities through full commercial supply, with a track record of consistent, audited performance for global pharma partners.
Recognized by the authorities that matter to your launch markets
Our Quality Management System is built around ICH guidelines and is 21 CFR compliant, with active accreditations across major regulatory markets.
CEP
PMDA
TGA
MOH
NMPA
MFDS
AIFA
- WHO-GMP certified & ISO 9001:2015 certified
- Compliance across IP, EP, BP, USP, JP & CP pharmacopoeial standards
- In-house AMV, PV and long/short-term stability studies
- EU Written Confirmation certificates across 35 products
- 21 CFR Part 11 compliant quality control systems
- Regularly audited by leading Indian and multinational firms
What we manufacture
Active Pharmaceutical Ingredients
Manufactured under WHO-GMP and ISO-certified processes, with PMDA and European regulatory approvals.
Chemical Intermediates
High-purity intermediates including sulphonyl chlorides, amides, acids and derivative.
Specialty Fine Chemicals
Complex organic molecules built to precise specification for synthesis and research applications.
Vitamin D3 Analogues
Premium analogues for calcium regulation and specialized therapies.
VIEW APIs →
Products in Pipeline
Emerging molecules and innovative solutions under active development.
VIEW APIs →
One partner, four specialized facilities
D.K. Pharma Tech Pvt. Ltd.
Dedicated CDMO facility specializing in hydrogenation and multi-reaction capability.Sagitta Pvt. Ltd.
Advanced multi-step intermediates, specialized in high-pressure oxidation.D.K. Bio Pharma Pvt. Ltd.
Advancing into oncology therapeutics, including single-dose formulation R&D.Eco Green Industries Pvt. Ltd.
Recycling and biofuel production, supporting our clean chemistry commitments.Relationships measured in decades, not deliverables.
Teva
Sanofi
Bayer
Lonza
“Deals begin with handshakes, not signatures.”
D.K. Pharmachem · Founding Philosophy1980 to today
Foundation
Founded by Dr. Rakesh Bakshi, starting with intermediates.Specialty Chemicals
Expanded into specialty and fine chemicals production.Advanced Intermediates
Introduced advanced intermediates for the global pharmaceutical industry.API Production
Began manufacturing APIs and bulk drug products.Vitamin D3
Added Vitamin D3 analogues to the product portfolio.Sagitta Pharma
Integrated Sagitta Pvt. Ltd., expanding production footprint.D.K. Bio Pharma
Welcomed D.K. Bio Pharma, strengthening the pipeline.New API Block
Built new API block, enhancing capacity and innovation.D.K. Pharma Tech
Launched D.K. Pharma Tech, advancing CDMO capability.— CDMO & Contract Manufacturing Services
Four decades of process chemistry, built for your supply chain.
WHO-GMP certified manufacturer of APIs, advanced intermediates and specialty fine chemicals — trusted by Teva, Sanofi, Bayer and Lonza for 15–20 years running.