Pharmaceutical automation engineered for precision, compliance, and scale
AIR partners with leading pharmaceutical companies to design, build, and support advanced automation systems for complex, highly regulated production environments. From product handling, filling, inspection, packaging, and serialization to full-line integration, we bring the engineering depth, project discipline, and scale needed to deliver high-performance solutions with confidence.
Why AIR for pharma
End-to-end partner
Deep, agile collaboration and 360 support — from ideas to concepts, build to commissioning, maintenance to optimization.
AIR is proud to support some of the world’s most advanced production teams in the pharma industry.

Pharma sector capabilities
Pharmaceutical process and product experience
AIR brings together deep automation expertise, proven project delivery, and the scale to support complex pharmaceutical programs from concept through commissioning and lifecycle support.
Pharmaceutical capabilities
Pharmaceutical manufacturing expertise
- Ultrasonic welding, adhesion, bonding, and lamination
- Laser process development and integration
- Custom lyophilized bead handling and automation
- Precision dispense of low and high-viscosity fluids
- Solid bead and powder reagent fill
- Aseptic environment compliance
- Precision alignment, orientation, feed, and assembly
- Defect inspection, sort, bin
- Clinical trials drug processes
Pharmaceutical packaging & packing expertise
- High-throughput robotic pick and place
- Testing and inspection
- Labeling and verification
- Serialization and track & trace
- High-speed product packaging
- High-speed product handling
Certification and standards excellence
- CGMP regulations, as enforced by the FDA
- ISO class 7 & 8, cleanroom equipment
- ATEX & high-temperature environments 200°C+
- Sealed nitrogen environments
- Computer validation system in compliance with GEP/GMP regulations
- Qualification system in line with GAMP requirements
- Hardware and software systems validated to GAMP-5
- FDA mandatory Unique Device Identifiers (UDI) regulations
- EU Medical Device Regulations (MDR) 2017/745
- TÜV SÜD validation
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Pharma case studies
A leading pharmaceutical company needed an automated solution capable of applying tamper-evident labels and unique device identification (UDI) labels to a variety of pharmaceutical cartons at high speed.
Scotland’s Medicines Manufacturing Innovation Centre (MMIC) required a manufacturing system capable of rapidly introducing new medicines into clinical trials while maintaining pharmaceutical hygiene…
Insights
Innovating the future of pharma production
An innovative single-line platform to significantly reduce time-to-market for new medicines