RADWAG PS 3500.5Y.M PS 5Y.M Precision Balance, 3500g Capacity, 10mg Readability, 21 CFR Part 11, Internal Calibration

RADWAG PS 3500.5Y.M Precision Balance — 21 CFR Part 11 Compliance on a 3500 g Platform

Regulated laboratories in pharmaceutical and biotechnology sectors demand instruments that support electronic record integrity. The RADWAG PS 3500.5Y.M Precision Balance pairs 3500 g capacity and 10 mg readability with 21 CFR Part 11 compliance, automatic internal calibration, and a 10-inch touchscreen equipped with the ReflexLEVEL automatic levelling system — making it ready for GxP environments straight from installation.

Key Features

• 21 CFR Part 11 Compliance: Supports electronic signatures, audit trails, and user access controls required by FDA regulations for electronic records in pharmaceutical workflows.
• 3500 g Capacity at 10 mg Readability: A broad weighing range with sufficient resolution for formulation work, raw material checks, and in-process quality sampling.
• Automatic Internal Calibration: Maintains traceability by self-calibrating at programmable intervals or in response to environmental changes, generating GLP-compliant reports.
• 10-Inch Touchscreen with Widgets: Customizable home screen widgets display real-time data, statistics, and process information, allowing operators to tailor the interface to their specific workflow.
• ReflexLEVEL Automatic Levelling: Motorized levelling eliminates manual adjustment, saving time and ensuring the balance operates within its specified accuracy at all times.

Detailed Overview

The PS 3500.5Y.M achieves linearity of ±20 mg and standard repeatability of 5 mg at 5 % load, providing consistent performance across the full 3500 g range. Semi-automatic LevelSENSING works in tandem with the ReflexLEVEL system to maintain optimal orientation continuously. Connectivity includes USB-A, USB-C, Ethernet, Wi-Fi, and Hotspot, enabling secure data transfer to validated LIMS or ERP platforms. The instrument's database engine stores user profiles, product libraries, and SOP definitions locally, streamlining regulated weighing processes. With 21 CFR Part 11 features active, every measurement is traceable to a specific user, time, and instrument state.

Applications

• Pharmaceutical manufacturing and GMP production environments
• Biotechnology research requiring validated data records
• Regulated chemical compounding with audit trail requirements
• Clinical trial material preparation and documentation

Why Choose this precision balance?

When your laboratory operates under FDA or equivalent regulatory oversight, the PS 3500.5Y.M provides the compliance infrastructure your weighing data needs. Combined with high capacity, automatic calibration, and a modern touchscreen, it removes barriers between precise measurement and regulatory readiness. Order today and bring validated weighing to your regulated facility.