Automation in Pharmaceuticals
Pharmaceutical & Biotech
POA delivers integrated control systems for pharmaceutical and biotech facilities, ensuring compliance while maintaining reliability.
Compliance should not wait
Your facility operates under constant FDA and GMP scrutiny while racing to bring therapies to market. Every system needs bulletproof documentation and single-source accountability without the vendor coordination nightmare.
+ Complex regulations trigger costly audit findings
+ Multiple vendors create documentation gaps
+ Limited staff struggles with CTE management
+ Cost pressure threatens quality standards
One reliable partner
We understand that in pharmaceuticals and biotech, documentation isn't paperwork, it's proof of patient safety. POA integrates automation expertise with deep regulatory knowledge.
Complete CTE Lifecycle Management
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We handle your controlled temperature environment program from specification through retirement—including cold rooms, stability chambers, -80°C freezers, incubators, and LN2 systems.
FDA & GMP-Compliant Documentation
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Our validation team authors User Requirement Specifications, Functional Specifications, and complete IQ/OQ/PQ protocols that pass auditor scrutiny on the first review.
Integrated Clean Room Systems
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We design and validate complete clean room automation including HEPA filtration qualification, environmental monitoring, pressure differential controls, and particle counting systems—all with 21CFR Part 11 compliant data management.
Simplify pharmaceutical compliance
Contact POA to discuss how our integrated automation and validation expertise eliminates vendor coordination headaches while delivering systems that pass audits the first time.
Complete pharma solutions
From initial system design through ongoing support, POA delivers integrated automation and compliance services.
Integration
Design and build complete automated systems with proper specifications, control panels, and programming—ready for validation from day one.
Calibration
NIST-traceable calibration and asset management keeping your instrumentation accurate, compliant, and audit-ready throughout the year.
Validation
Comprehensive testing and documentation proving your systems meet FDA, GMP, and ISO requirements with evidence auditors accept.
"I have had the pleasure of working with Steve, [Lonnie, Edie] and the rest of the POA team for nearly 24 years now.
From filtration and calibration to validation and systems integration, POA has the staff, experience, and knowhow to deliver high quality results."
Ian Stout
Serán Bioscience
"POA is a critical partner in the continued success of our mobile gas generation project. Their team has consistently demonstrated exceptional technical leadership while providing deep industrial automation expertise that has directly influenced the quality, reliability, and performance of our system."
Tim Kemper
Director of Engineering, CV International
"Working with POA has felt less like engaging a vendor and more like adding trusted teammates to our project. Their professionalism, organization, and commitment to doing things right have made a lasting impact on our success."
Tim Kemper
Director of Engineering, CV International
"In February 2015, the McKesson drug distribution facility in Memphis, Tennessee experienced a roof collapse due to an ice storm. The damage...(threatened) the CDC's entire US supply of vaccines for children. With Steve and Lonnie leading, the entire POA team provided 24/7 support to McKesson. With POA's collaboration, McKesson was able to stabilize the situation, install a new controller, and get it operational. In this situation, partnering with the right company saved McKesson from a potential $876,000,000 loss."
Timothy Phelps, McKesson
Former Manager of Facilities & Engineering