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Drug Logix India Private Limited
Infrastructure

Built for chemistry. Engineered for scale.

R&DDriven Chemistry

An integrated approach to product development.

At Drug Logix India, our integrated product development approach is designed to meet every business requirement. Supported by a state-of-the-art R&D facility, our expert teams work in tandem to drive new product introductions and process innovations to global standards.

Our product development expertise bridges advanced science and strategic execution, encompassing synthetic organic chemistry, analytical chemistry, process engineering, intellectual property management, project management, and regulatory science.

We are committed to injecting innovative thinking at every stage of the pharmaceutical value chain. By continuously optimizing processes for cost-efficiency, we help our partners propel their medicines to market faster, maintain a fierce competitive edge, and ensure long-term business sustainability.

Talk to Our Chemists

Analytical depth, characterisation precision.

Drug Logix India outsources analytical laboratory services for the development of analytical methods to evaluate the quality of raw materials, API intermediates, key starting materials, and impurity reference standards — with a specific focus on genotoxic impurities, nitrosamines, NDSRIs, and other trace contaminants.

Chromatography & Mass Spectrometry

LC/MS-MS, Preparative HPLC, HPLC, UPLC, GC, and GC/MS.

Spectroscopy

NMR (400 MHz and 500 MHz) and FTIR.

Thermal Analysis

DSC and TGA.

Wet Chemistry

Fully equipped for classic wet analytical methods.

From bench to kilo-lab.

Drug Logix India has a Memorandum of Understanding (MoU) with an external provider in Hyderabad for scale-up of our products ranging from 0.5 Kg to 5 Kg.

The reactor capacity ranges from 20 L to 200 L.

0.5 – 5 KgScale-up Range

Two cGMP facilities. Global approvals.

Drug Logix India has a Memorandum of Understanding (MoU) with two Global Regulatory agency-approved plants in Hyderabad for commercialization of our API intermediates and key starting materials (KSMs). Two cGMP compliance manufacturing facilities are located in Hyderabad, India.

Each manufacturing facility is designed, equipped and operated to deliver high quality products within defined cost and delivery schedules. We have capabilities in a wide range of API intermediates and have handled varied process reactions and reactor volumes exceeding 400+ KL.

We strictly adhere to worldwide safety, health, and environmental standards and our manufacturing facilities are ISO certified.

Approved by Global Regulatory Agencies

USFDA EU-GMP TGA Japan PMDA CDSCO-India WHO-GMP

Equipped for complex chemistry.

Our manufacturing facilities are equipped with sophisticated capabilities to carry out multiple reactions.

Cryogenic reactions up to −70°C
Grignard chemistry
Chlorination
Bromination
Oxidation
Nitration
Amination
Esterification
Amidation
Reduction
Methylation
Metal reactions (Butyl Lithium, Sodium metal etc.)
Hydrogenation reactions
In situ reactions etc.

Want to visit our facility?

We welcome audits and site visits from existing and prospective clients. Schedule a walk-through of our R&D Centre and manufacturing units.

Schedule a Visit