Struggling with manual weight loss calculations, cumbersome drum emptying procedures, or testing larger tablets that slide rather than tumble? Pharmaceutical quality control laboratories frequently face the challenge of evaluating uncoated dosage durability under strictly prescribed pharmacopoeial conditions. Implementing an advanced Friability Tester FRV 210i testing platform directly resolves these workflow hurdles by combining automated weight loss calculations with an exceptionally intuitive touchscreen interface. This ensures absolute quality and physical resilience of your dosage forms while completely eliminating manual math errors.

Technical Specifications

• Model Number: FRV 210i

• Compliance Standards: Fully complies with Ph. Eur. 2.9.7 and USP <1216> pharmacopoeial standards

• Drum Capacity: Supports up to two friability and/or abrasion drums simultaneously

• Tablet Compatibility: Specifically optimized for uncoated tablets

• Unit Dimensions: 407 by 343 by 325 millimeters including drums

• Control Interface: Intuitive touchscreen control for simplified daily operation

• Angling Mechanism: Built-in 10 degree angling device to accommodate larger tablets

• Data Output Interfaces: RS 232, USB A, and USB B ports standard

• Weighing Function: Optional automated weighing function utilizing a 3 d.p readable Ohaus Balance

• Equipment Certification: Certificate of Compliance provided as standard

Key Benefits and Solving Lab Challenges

Quality assurance technicians often lose critical time executing manual weight loss calculations or dealing with equipment that cannot easily accommodate non-standard tablet sizes. This device completely eliminates these operational pain points. By utilizing a reliable Friability Tester FRV 210i automated system, operators benefit from an integrated calculator that automatically determines the exact percent of tablet weight loss. This guarantees perfectly reproducible testing records and entirely removes human transcription errors from your evaluation process.

Workflow inefficiencies during high-volume testing are major vulnerabilities for any facility aiming for uninterrupted production. This instrument actively prevents testing delays through its convenient drum emptying design, which vastly streamlines the batch-to-batch turnover rate. The comprehensive capabilities of the Friability Tester FRV 210i allow users to quickly output their secure results and analytical reports directly to a PC or printer, ensuring maximum data integrity and strict audit readiness.

Core Operational Features

Every unit is engineered to maximize testing throughput while maintaining strict compliance with global pharmacopoeia manufacturing standards.

• Intuitive Touchscreen Operation: The bright display simplifies method setup and execution, drastically reducing the required training time for new laboratory personnel.

• Built-in Angling Device: Easily tilts the instrument to a 10 degree angle, preventing larger tablets from sliding and ensuring they tumble correctly for accurate abrasion results.

• Comprehensive Documentation: Supported by available IQ/OQ/PQ documentation packs and qualification tools, acting as a compliant Friability Tester FRV 210i analytical instrument for highly regulated environments.

• Versatile Accessory Integration: Easily adapts to your specific workflow with optional abrasion drums, integrated printers, and precision balances for a fully automated testing loop.

Upgrade Your Quality Control Workflow

Modern pharmaceutical manufacturing demands instruments that deliver uncompromising accuracy, rapid sample processing, and absolute regulatory compliance. Integrating a top-tier Friability Tester FRV 210i into your quality control regimen ensures your facility remains highly efficient and your final products survive the harshest packaging and transportation environments. Invest in an industrial-grade physical testing solution today to streamline your complex material evaluation protocols, eliminate costly operational downtime, and achieve absolute confidence in every single drug batch.