Pharma Automation Compliance
Compounding Pharmacies
POA supports compounding pharmacies with automation and validation systems that ensure GMP and FDA compliance.
Small scale with high standards
Pharmacies faces the same stringent USP 795, 797, and 800 requirements as large manufacturers, but with limited staff and budget. Every clean room and controlled environment needs proper validation, and documentation without the overhead of a full quality department.
+ USP regulations require strict environmental control
+ Limited staff handles production and compliance
+ Clean room certification costs strain budgets
+ Documentation gaps trigger inspection failures
One reliable partner
We design automation systems that protect product safety while increasing efficiency. Our team is trained in FDA Good Manufacturing Practices and understands food-grade requirements.
USP 797 Clean Room Systems
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We design and validate complete clean room environmental monitoring including ISO classification verification, particle counting, differential pressure monitoring, temperature and humidity control.
USP 800 Hazardous Drug Controls
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Negative pressure room controls, containment ventilation monitoring, and environmental sampling support ensuring safe handling of hazardous drugs with proper documentation and compliance verification.
Controlled Temperature Environments
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Refrigerator and freezer monitoring for ingredient storage, compounding area temperature control, and beyond-use date environmental validation maintaining product stability and regulatory compliance.
Simplify USP compliance
Contact POA to discuss how our right-sized automation services will help you meet USP requirements without enterprise-level costs.
Complete industry solutions
From clean room design through ongoing monitoring, POA delivers integrated automation for compounding pharmacies.
Integration
Design and install environmental monitoring systems with proper controls, alarms, and data logging—ready for clean room certification.
Calibration
NIST-traceable calibration and asset management keeping your monitoring equipment accurate and maintaining compliance year-round.
Validation
Clean room certification, equipment qualification, and temperature mapping documentation proving your facility meets USP requirements.
"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