API & Intermediate Manufacturing

Precision in
Every Molecule
We Produce

SHARIKA Life Science is a trusted manufacturer of Active Pharmaceutical Ingredients and advanced intermediates, delivering quality at scale for the pharmaceutical industry.

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Years in Operation

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APIs & Intermediates

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Skilled Workforce

About SHARIKA

Built on Expertise. Driven by Quality.

SHARIKA Life Science Limited is a leading API and pharmaceutical intermediate manufacturing company, situated on a 20,614 sq. m site in designated Industrial Area, midway along Delhi-Jaipur Highway, with a 5,100 sq. m ground built-up area. Our current infrastructure provides a volumetric capacity of 93 KL alongside two fully operational cleanrooms, and we are ready to expand by another 300 KL (or more) and two additional cleanrooms based on current completed construction.

Specializing in Hydrogenation, Bromination, and Chlorination, our integrated manufacturing campus houses multi-purpose production blocks capable of handling a wide range of complex and highly hazardous chemistry. We serve as a reliable partner from lab-scale development through to commercial manufacturing.

Every batch we produce reflects our commitment to regulatory compliance, operational excellence, and the highest standards of safety and environmental responsibility.

As per Revised Schedule M GMP Certified
ISO Certified
Eco-Compliant
Our Facility

World-Class Manufacturing Infrastructure

Our purpose-built facility handles complex chemistry at scale, with dedicated zones for hazardous reactions, clean room operations, and rigorous contamination control.

Bromination

Dedicated bromination bay with scrubber systems, bromine-resistant piping, and temperature-controlled reactors for safe handling of reactive bromine chemistry.

Reactor Range4000L
MaterialGlass-Lined
Temp Control-30°C to 200°C
ScrubberCaustic

Hydrogenation

Purpose-built hydrogenation block with pressurized autoclaves, hydrogen storage and distribution system, and comprehensive safety interlocks.

Pressure RangeUp to 24 bar
Vessel Capacity1000 L
Catalyst HandlingDedicated filtration
SafetyBurst disc + RPG

GLR & Reactors

Multi-purpose glass-lined and stainless steel reactors for diverse reaction types including condensation, alkylation, nitration, and reduction.

GLR Reactors3000L – 6000L
SS Reactors3000L – 8000L
AgitationAnchor / Turbine
Total Vessels25+

Clean Rooms

Controlled-environment clean rooms designed for sensitive API handling, final product isolation, drying, and packaging — maintaining compliance with EU-GMP and WHO-GMP particle and microbial limits.

ClassificationISO Class D
HEPA Filtration99.97% @ 0.3µm
Air Changes20–60 per hour
MonitoringReal-time particle counter

R&D and Quality Control

Our in-house R&D center provides complete process scale-up capabilities, supporting development from gram to kilogram scale. Alongside this, our fully equipped QC and microbiology laboratory utilizes state-of-the-art analytical instruments to ensure every product meets stringent pharmacopoeial standards.

HPLC

Purity & assay testing

Gas Chromatography

Residual solvent analysis

FTIR / NMR

Structural confirmation

Malvern

Accurate Particle Analyzer

Nitrogen Generation

On-site PSA nitrogen plant for inert atmosphere in reactors, blanketing, and transfer operations.

Solvent Recovery

Dedicated in-house solvents recovery facility ensuring sustainable and cost-effective operations.

Effluent Treatment

Zero Liquid Discharge (ZLD) system managed with advanced SCADA-based utilities.

Warehouse & Logistics

Temperature-controlled storage with segregated areas.

Products & Business

What We Offer

From custom synthesis to commercial-scale API manufacturing, our business model supports pharmaceutical companies at every stage without any greenfield delay.

Custom Synthesis

Multi-step synthetic routes for novel intermediates and API's from gram to multi-kilogram scale.

Route scouting & optimization
Gram to 100 kg scale
Complete analytical package

CDMO Services

End-to-end development and manufacturing partnerships with regulatory filing support.

Process validation (PPQ)
DMF / ASMF support
Long-term supply agreements

Regulated Market API's

Commercial manufacture of API's compliant with regulated markets with documentation support.

EU-GMP/USFDA compliant
ICH stability studies
Regulatory inspection ready

Contract Manufacturing

Cost-effective toll manufacturing with full confidentiality and IP protection.

Your process or ours
NDA & CDA protected
Competitive pricing at scale

A Plug-and-Play Asset for Your Growth

We believe this asset is a plug-and-play fit for organizations looking to add regulatory-approved API capacity with no greenfield delays, or expand CDMO operations with the ready infrastructure.

Contact Us

Let's Discuss Your Requirements

Manufacturing Site & Head Office

SHARIKA Life Science Limited
SP1-6B, RIICO Industrial Area,Sotanala
Behror, Rajasthan, INDIA

Business Enquiries

info@sharikalife.com

Phone

01494-294111

Enquiry Sent

Our team will respond within 24 hours.