Fully automated compounding system RIVA®

for laboratory automationmedicalfor liquid handling

Overview
RIVA® is a fully automated IV compounding system purpose-built to prepare sterile IV syringes and IV bags. It handles hazardous and non-hazardous preparations, providing automated workflows to improve medication safety, accuracy, traceability and operational efficiency.

Key Capabilities

• Automated preparation of sterile IV syringes and IV bags
• Supports hazardous and non-hazardous drug compounding
• Barcode-verified label generation when integrated with Codonics Safe Label System (SLS)
• Complete electronic audit trail for traceability and regulatory documentation

Compliance & Safety
Designed to help hospitals maintain compliance with USP <797> and USP <800> compounding chapters. RIVA aligns with NIOSH and OSHA guidance and is North American safety listed and CE marked.

Operational Benefits

• Precision and reproducibility to reduce dosing and labeling errors
• Reduced human error and contamination risk through robotic accuracy
• Reduced pharmaceutical waste via optimized batch sizes and extended beyond-use dating
• Lower labor and operational costs by automating repetitive tasks
• Consistent throughput with minimal downtime to support long-term savings

Integration & Labeling
Integrates with hospital label and drug database systems to enable full-color, barcode-verified labels (e.g., Codonics SLS) that match approved hospital drug databases—minimizing medication identification errors and standardizing OR medication labeling.

Use Cases & Evidence
Used in hospital pharmacy environments for aseptic compounding of IV medications and syringes. Provides end-to-end documentation and traceability for each dose prepared. Promotional materials reference milestone production volumes exceeding millions of sterile doses.

Available Resources
RIVA Fact Sheet, RIVA Datasheet, RIVA Vancomycin Case Study, GMP RIVA Key Features for Regulatory Compliance

Technical specifications

• Product name: RIVA®
• Intended preparations: Sterile IV syringes and IV bags
• Handles: Hazardous and non-hazardous drugs
• Regulatory support: Designed to support USP <797> and USP <800>
• Standards & certifications: NIOSH/OSHA-aligned guidance; North American safety listed; CE marked
• Traceability: Full electronic audit trail per dose
• Integration: Supports integration with labeling systems (e.g., Codonics Safe Label System)
• Operational focus: Reduced human error, reduced waste, optimized batch sizes, consistent throughput
• Documented materials: Fact sheet, datasheet, case studies and regulatory feature documentation available as PDFs