OUR GMP SUITES
Scalable, Compliant Manufacturing Solutions
Designed with regulatory compliance and process scalability at their core, our cleanroom facilities provide the ideal environment for clients across the biotech and pharmaceutical sectors.
Our Facilities
Parimer's GMP suites are purpose-built to support the development and manufacture of a wide range of therapeutic modalities. Our modular cleanroom environments meet ISO Class 7 and 8 standards and include dedicated HVAC systems for contamination control and suite separation.
Total facility: 6,000 sq ft
Cleanroom suites: ISO 7 and ISO 8
Containment: Pressure differential and HEPA air handlers
Environmental monitoring: Particle and VOC counting
Integrated Equipment for Precision Production
Our GMP facilities are supported by a robust suite of in-house equipment, enabling high-quality, reproducible manufacturing runs. Key resources include:
Batch chemical reactors (100 mL – 600 L)
Pharmaceutical basket centrifuge
Non-metallic filter presses (up to 20 kg solid batch capacity)
High-purity gas generation (O2, N2, H2) for inert atmospheres
USP-grade RO water systems for formulation and cleaning
Milling, blending, drying, and other particle processing tools
To view our complete equipment list
Core Capabilities
Our GMP suites support end-to-end chemical or pharama workflows:
Process Development & Scale-Up
Clinical material production and purification
Primary packaging
Analytical Testing & Quality Control
Technology Transfer & Batch Documentation Support
Whether you're transitioning from early-stage R&D or preparing for GMP batch production, Parimer can support you every step of the way.
Facility Design & Workflow
Built for flexibility and speed, our GMP suites features:
ISO Class 7/8 cleanrooms with flush finishes
Gowning rooms and airlocks for controlled personnel entry
Segregated HVAC systems for product and personnel flow
Hazardous vapor ventilation control
Why Choose Parimer?
From project scoping to GMP batch execution, we partner closely with your team to:
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Evaluate process requirements
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Define production timelines
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Develop or adapt standard operating procedures
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Ensure regulatory readiness and documentation