
Life Sciences
Automation systems built for validated, traceable, and audit ready production
Scalable automation that optimizes capital spend while reducing implementation risk.
As medical device and pharmaceutical manufacturers are challenged to scale manufacturing to meet demand, Integrion Automation has the experience to help guide you in developing a volume ramp up strategy that optimizes your capital spend over time.
Regardless of if you are preparing for pilot production, preparing for new product launch, needing to increase volumes of existing product or looking to optimize the OEE of existing equipment, we would appreciate the opportunity discuss your needs and how we can help!
Life Science Applications
- Diagnostics
- Diabetes Care
- IV Tube Sets
- Vision Care
- Wearable Devices
- Orthopedics
- Surgical Devices
- Catheters
- Medical Filters
- Bio Processing Bags
In life sciences manufacturing, automation has to do more than move parts. It needs to protect product integrity, support traceability, and deliver consistent quality in highly controlled environments. Integrion Automation designs and integrates systems that reduce manual handling, improve inspection reliability, and keep production running with documentation-ready processes and lifecycle support.

Integrion Automation prides itself on predictable and professional project execution.
Process Experience
Data & Traceability
High Precision Automated Assembly
Inspection & Testing
Integration & Machine Tending
Material Handling & Palletizing
Part Feeding
Part Joining
Precision Cutting
Precision Motion & Tooling
Vision Based Active Alignment
Web Handling
Pre-Automation Services
Integrion Automation brings a life-sciences mindset to every build: disciplined project execution, documentation ready delivery, and systems engineered for repeatability.
These value-add services are how we keep projects predictable from concept through validation support and long-term uptime.
- Develop equipment specifications
- Volume ramp-up strategy
- Planning and budgeting
- ROI calculations
- Automation Assessment
- Process risk assessment
- Proof of principle
- Process development assistance
- Design for manufacture recommendation
- Robot and line simulations
Compliance, Validation & Quality
We design with validation in mind—documentation-friendly, traceable, and aligned to GAMP best practices to streamline your path to approval.
Integrion Automation is ISO 9001 certified with experience in current Good Manufacturing Practices (cGMPs). We follow GAMP 5 recommended documentation practices to reduce timing in IQ/OQ execution and keep your project on track.
Documentation we deliver:
• Traceability Matrix
• FMEA
• Functional Specification
• Design Specification
• Validation Acceptance Test Plan
Design considerations built in:
• Design for cleanability
• Clean room compatibility

Real Projects. Real Results.
Explore how we've helped life sciences manufacturers solve complex challenges and hit their production goals. From case studies and project highlights to insights from our engineering team see what's possible when experience meets execution.

Our Life Sciences Offerings
Field Service & Lifecycle Support



