Proveris Scientific SprayVIEW - Measurement Systems for OINDP Testing
The SprayVIEW Measurement Systems by Proveris Scientific serve as a pivotal tool in the meticulous analysis and validation of orally inhaled and nasal drug products (OINDPs). Designed to adhere to stringent industry standards, these systems enable precise measurement of spray patterns and plume geometries generated by various spray and aerosol devices. Trusted by leading pharmaceutical firms, contract development, manufacturing, and research organizations, as well as regulatory bodies globally, the system offers robust data critical for pre-submission assessments and production testing. Featuring the versatile Vereo Automated Actuators, it supports semi-automated analysis essential for FDA compliance concerning bioequivalence assessments. Additionally, it facilitates comprehensive product characterization by assessing attributes like plume velocity and evaporation rates. The system is augmented by the Viota Software, providing a seamless user experience with advanced data analysis, method development, and compliance with electronic record regulations, thereby enhancing operational accuracy and efficiency.
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semi-automated analysis of spray pattern and plume geometry required by U.S. FDA compliance documentation (2003 BA/BE Draft Guidance)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