Industries

PHARMACEUTICAL / BIOPHARMACEUTICAL

Purity Engineered for Compliance & Efficiency

Pharmaceutical manufacturing demands uncompromising quality. From high-purity water to specialized purification processes, every step must align with stringent global regulations — USFDA, WHO, UKMHRA, TGA, and beyond. Nilsan Nishotech delivers end-to-end solutions that ensure product safety, regulatory compliance, and operational reliability.

Biopharmaceuticals require extremely sensitive and specialized purification processes. Our solutions are designed to handle complex biomolecules with maximum recovery and stability, ensuring consistent yields for high-value biologics.

Interactive Solutions

High Purity Water Systems – USP, EP, and JP compliant

cGMP-compliant designs meeting pharmacopoeia standards Ensures consistent water quality for sterile manufacturing environments. Designed to meet USP, EP, and JP requirements with automated sanitization and validation protocols. Delivers reliable operation with minimal downtime.

Plasma Fractionation – Optimized separation of plasma proteins

Designed for precise recovery of albumin, immunoglobulins, and clotting factors. Maintains protein integrity while meeting stringent GMP guidelines. Scalable for both clinical and commercial production.

Recombinant Protein Purification – Gentle yet precise processes for stability

Utilizes tailored chromatography and filtration techniques to preserve bioactivity. Ensures consistent molecular structure across batches. Ideal for therapeutic proteins requiring high stability and low impurity profiles.

Monoclonal Antibody (mAb) Purification – Consistent product quality at scale

Delivers high-yield antibody recovery with uniform glycosylation profiles. Incorporates multi-step chromatography for precise impurity removal. Validated for large-scale GMP production with reproducible outcomes.

Fermentation Broth Extraction – High-throughput clarification and separation

Efficiently removes cells, debris, and particulates from complex fermentation mixtures. Maintains product potency while reducing downstream processing time. Compatible with a variety of microbial and mammalian expression systems.

Pyrogen Removal

Endotoxin-free processing for critical products Ensures compliance with strict injectable and ophthalmic product standards. Employs proven membrane and thermal technologies for safe production. Critical for patient safety and regulatory approvals.

Case Study

Challenge:

A leading pharma company faced inconsistent water quality in peak production.

Solution:

Installed an integrated NeroSOFT + NeroLOOP system with automated sanitization.

Result

35% reduction in downtime, full compliance in all audits.

Complete Injectable Process Plant (LVP & SVP)

Comprehensive system for sterile production of Large Volume Parenterals (LVP) and Small Volume Parenterals (SVP).

Formulation vessels, filtration & sterilization units, aseptic transfer systems, CIP/SIP automation, filling & sealing line.

Enables compliant, contamination-free manufacturing of IV fluids, injectable drugs, and vaccines.

Ointment Manufacturing System

Integrated solution for producing ointments, creams, gels, and lotions with hygiene and consistency.

Includes water & oil phase vessels, main mixer, homogenizer, vacuum pump, discharge unit, and control panel.

Supports manual, semi-automatic, and fully automatic (CIP/SIP) configurations for scalable production.

Compliance

Let’s Build Your Industry Advantage

From pilot plants to full-scale manufacturing, Nilsan Nishotech delivers solutions that align with your industry’s toughest demands.

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