Pharmaceutical manufacturing demands automation that meets strict regulatory requirements, operates in clean room environments, and maintains complete traceability. AMD Automation provides validated solutions for drug packaging, device assembly, and laboratory automation.
Packaging Automation
Primary and secondary packaging systems:
- Vial filling, stoppering, and capping
- Syringe filling and assembly
- Blister pack and carton loading
- Serialization and aggregation with vision systems
Drug Delivery Device Assembly
Automated assembly for injectors and inhalers:
- Robotic assembly cells in clean environments
- Servo pressing for precision component insertion
- Automated testing for functionality verification
- Dispensing for lubricants and adhesives
Inspection and Quality
Vision and sensor-based quality systems:
- Machine vision for fill level and particulate inspection
- Label presence and print quality verification
- Dimensional inspection for device components
- Color and cosmetic defect detection
Clean Room Automation
Equipment designed for controlled environments:
- Stainless steel and clean room compatible materials
- Minimized particle generation
- Easy cleaning and sanitization
- Validated for pharmaceutical environments
Regulatory Compliance
AMD provides documentation for validation:
- IQ/OQ/PQ protocols
- 21 CFR Part 11 compliant data handling
- Full traceability and audit trails
- Risk assessment support
Related Industries
Pharmaceutical shares requirements with:
- Medical Devices - Assembly and packaging
- Food & Beverage - Filling and packaging
- Electronics - Clean room assembly
Contact us to discuss automation for your pharmaceutical manufacturing operation.
Automation Solutions for Pharmaceutical
Packaging Automation
Primary and secondary packaging for vials, syringes, bottles, and blister packs.
Assembly Systems
Clean room assembly for drug delivery devices and diagnostic equipment.
Inspection Systems
Vision inspection for fill level, particulate, label verification, and serialization.
Material Handling
Automated handling for vials, cartridges, and packaging materials.
Industry Challenges We Solve
Regulatory Compliance
FDA and international regulations require validated processes with full documentation.
Clean Room Requirements
Manufacturing environments must maintain strict particulate and contamination control.
Product Traceability
Serialization and track-and-trace requirements demand complete batch documentation.
Let's discuss your specific automation challenges.