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Pharma Industry

Pharma Industry compressed air solutions
Air Solutions for Pharmaceuticals

Pharmaceutical-grade compressed air — clean, validated, GMP-compliant

Compressed air in pharmaceutical manufacturing is classified as a direct or indirect product contact utility, making air quality a regulatory requirement, not just a preference. AP Compressors supplies and configures compressed air systems with oil-free quality output, validated desiccant drying, and multi-stage filtration appropriate for tablet presses, blister packaging, capsule filling, liquid dosage lines, and clean room instrumentation across pharmaceutical plants in Nepal.

  • Oil-free quality compressed air meeting ISO 8573-1 Class 1 for product-contact applications
  • Desiccant dryers achieving pressure dewpoints of –40°C for moisture-sensitive processes
  • Multi-stage filtration: particulate, coalescing, and activated carbon for complete contamination control
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What we provide

  • Oil-free quality compressed air meeting ISO 8573-1 Class 1 for product-contact applications
  • Desiccant dryers achieving pressure dewpoints of –40°C for moisture-sensitive processes
  • Multi-stage filtration: particulate, coalescing, and activated carbon for complete contamination control
  • Stainless steel receiver options and sanitary-grade fittings for GMP-sensitive installations
  • Full system documentation for validation and regulatory review
  • Redundant compressor configurations maintaining uptime in continuous pharmaceutical production
  • Periodic air quality testing and system audits to support ongoing GMP compliance

System overview

Typical Pressure6 – 10 bar
Key EquipmentScrew compressor, desiccant dryer, multi-stage filters
Air QualityISO 8573-1 Class 1 (GMP-grade)
Dewpoint–40°C pressure dewpoint
DocumentationAvailable for validation protocols
ServiceAMC, filter validation, air quality monitoring

Key applications

1

Tablet Pressing & Coating

Tablet presses and coating pans use compressed air for material conveying, pneumatic actuation, and spray guns. Product-contact air must meet strict oil and moisture limits.

2

Capsule Filling

Capsule filling machines use compressed air for dosator actuation, capsule separation, and dust extraction. Contaminated air directly affects fill accuracy and product integrity.

3

Blister Packaging

Blister forming and sealing lines use compressed air to drive forming plugs, heat seal actuators, and indexing mechanisms. Clean, dry air prevents packaging defects.

4

Liquid & Injectable Lines

Liquid dosage and injectable manufacturing lines require the highest air quality standards — any contamination risk in product-contact airstreams is unacceptable under GMP.

5

Instrumentation & Clean Rooms

Instrument air for control valves and clean room pressurisation requires consistent pressure, low dewpoint, and zero oil contamination.

Why AP Compressors

Compressed air specialists with deep experience in pharma industry

AP Compressors doesn't just supply equipment — we design, install, commission, and support the full compressed air system for your facility, backed by a nationwide service network across Nepal.

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Turnkey supply, installation, and commissioning across Nepal

Rotary screw and PM VFD compressors matched to your exact CFM and pressure needs

Aluminium and MS pipeline networks for clean, low-pressure-drop air distribution

Refrigerated and desiccant drying for moisture-sensitive processes

AMC packages with scheduled maintenance and priority breakdown response

Genuine OEM consumables — filters, separators, oil — for maximum equipment life

Support & Answers

Frequently Asked Questions

Find answers about our air compressors, air dryers, filters, customized compressed air solutions, installation, and maintenance services.

Reach out to our team

Direct product-contact air typically requires ISO 8573-1 Class 1 for oil content (≤0.01 mg/m³) and Class 1 for moisture. Indirect contact and utility air may permit Class 2. Your validation protocol will define the exact requirements for each use point.

Yes. We can provide equipment data sheets, filter specifications, and system schematics to support your IQ/OQ validation documentation. Discuss your specific validation requirements with our team.

Most GMP guidelines require periodic air quality testing — typically annually or following any significant system change. We offer air sampling and testing services to support your ongoing compliance programme.

Yes. We design N+1 redundant configurations with duty/standby compressors, automatic changeover, and common distribution to ensure continuous air supply for uninterrupted production.

Get in Touch

Need compressed air for your pharma industry operation in Nepal?

Share your location, process requirements, and we'll recommend the right system for your facility.

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