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Integrated Campus

Our Infrastructure

Explore Our Pharmaceutical Infrastructure

Integrated Campus

Our manufacturing unit is located at Positron Medical Park Campus, Kanpur, spread across 50,000 sq. meters in a non-polluting industrial area. The campus stands as the first integrated Pharma & Medical Devices Park in Uttar Pradesh, purpose-built to promote efficiency, sustainability, and technological advancement.

Advanced Infrastructure

At Positron Biogenics, our state-of-the-art infrastructure forms the foundation of our commitment to innovation, quality, and operational excellence. Designed to meet global pharmaceutical standards, our facility integrates advanced technology, automated systems, and optimized workflows to ensure precision and efficiency at every stage of production.

Modern Manufacturing

Our manufacturing unit houses modern equipment from globally recognized brands such as ACG, Russell, and Cadmach, all SCADA-enabled to maintain real-time monitoring and process control. With specialized areas for solid orals, semi-solids, and topical formulations, we ensure high-capacity output while maintaining stringent quality and safety protocols.

Controlled Environment

The facility is equipped with walk-in and stability chambers, dedicated AHUs and DHUs, and an in-house water purification system to support a controlled and compliant production environment. Each production line is designed for flexibility—allowing rapid scale-up and smooth integration of new product lines with minimal turnaround time.

Quality Assurance

Our infrastructure is further strengthened by robust inventory management systems and quality assurance protocols, ensuring consistent supply, full audit compliance, and minimal risk of operational disruptions. Every process—from concept to dispatch—is executed with precision, reflecting our commitment to building a healthier and more sustainable future through advanced pharmaceutical manufacturing.

MFG Capacity

Our Manufacturing Capacity

Solid Oral Dosage (Tablets):

  • Plain
  • Coated
  • Layered

Semi-Solid & Topicals:

  • Ointments
  • Gels
  • Roll-ons

Capsules:

  • Hard Gelatin Capsule
  • And Many More...

Production Capacity

  • Oral Solids : 166,000/hr
  • Roll-Ons : 3600/hr
  • Semi-Solids : 3600/hr
  • Packaging :29,400/hr

Advanced Facilities

Our manufacturing unit is equipped with top-class machinery from ACG, Russell, & Cadmach, all of which are SCADA-enabled, enabling us to manufacture high-quality formulations. We've built-in 1 walk-in & 2 stability chambers, 29 AHUs, 8 DHUs & an in-house water purify system.

Flexible Production

Our flexible production lines are engineered to adapt swiftly to new product introductions & higher output volumes, significantly reducing time-to-market. Additionally, our robust inventory management systems ensure supply chain continuity & reduce the operational disruptions risk.

Quality Driven

We are committed to delivering products that meet the highest standards of quality, ensuring safety at every stage, and proving efficacy through reliable results. Our foundation is built on trust, compliance, and excellence.

Audit compliance

We adhere strictly to regulatory guidelines and maintain transparent processes to ensure full audit compliance. Regular internal and external audits help us uphold the highest standards of quality, safety, and efficacy, fostering trust and accountability.

How We Work

From Concept to Creation — A Trusted Pharma-Journey

Our process is driven by innovation, precision and quality. From idea to product, every stage is guided by research excellence, stringent testing and seamless collaboration for reliable pharma results.

Step 01

Concept and Understanding

We begin by analyzing healthcare needs to design innovative, affordable, and impactful pharma solutions.

Step 02

Research & Development

Our R&D teams transform ideas into world-class formulations through advanced science and technology.

Step 03

In Process Quality Check

Every stage is monitored with precision and care to maintain global quality and safety benchmarks.

Step 04

Quality Assurance

Rigorous multi-stage testing and validation processes ensure every formulation meets WHO-GMP standards, global regulations, and our unwavering commitment to safety, consistency, and patient trust through continuous monitoring and improvement.

Step 05

Production

Our WHO-GMP-certified facilities utilize advanced technology, automated systems, and expert supervision to manufacture high-quality medicines and medical devices with precision, scalability, and operational excellence at every stage of production.

Step 06

Packaging

Each product undergoes secure, contamination-free packaging using advanced materials and controlled environments to maintain product integrity, stability, and purity until it reaches the end user worldwide with complete safety assurance.

Step 07

Dispatch

Finished goods are handled through an efficient, technology-driven distribution system ensuring safe logistics, full traceability, and timely delivery of healthcare products across India and trusted international markets with total reliability.