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Proveris SprayVIEW - Measurement Systems for Nasal and Oral Drug Products
SprayVIEW Measurement Systems by Proveris are industry-standard tools designed to evaluate the spray patterns and plume geometry of orally inhaled and nasal drug products (OINDPs). These systems are crucial for both development and quality control phases, ensuring compliance with FDA guidelines and providing bioequivalence assessments. The system's adaptability allows for its application across a range of OINDP devices, including inhalers and nasal sprays. Equipped with the robust Vereo Automated Actuators, these systems perform semi-automated analyses critical for understanding product performance. The included Viota Software facilitates precise instrument control, method development, and data analysis, enhancing compliance with 21 CFR Part 11 regulations. This comprehensive software comprises user-guided workflows and technical controls that aid in maintaining data integrity, while its connectivity to a central database supports method validation and deployment across various sites.
Designed to meet rigorous testing standards for orally inhaled and nasal drug products (OINDPs), SprayVIEW® Measurement Systems are the industry standard for measuring and analyzing the spray pattern and plume geometry produced by spray and aerosol generating devices.
These systems have been validated and are being used in development and production environments at leading pharmaceutical companies, CDO/CMO/CROs, device manufacturers, and regulatory agencies around the world.
Spray Pattern, Plume Geometry, and So Much More
- Single system for both development and QC offers valuable insight into product performance during your pre-submission phase, as well as day-after-day reliability for production lot release testing
- Configurable for a wide variety of OINDP devices from inhalers to nasal sprays by taking advantage of our family of:Vereo® Automated Actuators
- Provides robust, semi-automated analysis of spray pattern and plume geometry required by U.S. FDA compliance documentation (2003 BA/BE Draft Guidance)
- Accurate characterizations of reference products lets you achieve bioequivalence faster
- Helps you understand how Critical Quality Attributes (CQAs) such as formulation viscosity and pump/valve design affect your product’s performance
- Lets you measure plume velocity and evaporation rate for in-depth product characterization