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Proveris Scientific - Viota® Software

Viota® software easily keeps you in control of every aspect of your OINDP testing. The powerful, intuitive interface makes it simple to create methods, execute system runs, and analyze important data across all Proveris instruments.

Containing all the tools you need to achieve 21 CFR Part 11 compliance, the software eliminates paper record keeping, and lets you manage your data more efficiently. Use of a traditional client-server architecture ensures that data is collected and stored safely and securely, and available for analysis any time, anywhere.

Key features

  • Industry-leading Viota software offers intuitive instrument control, method development, data analysis tools, as well as a full audit trail for your product
  • Intuitive, user-guided workflows ensure quality data generation and minimize errors
  • Comprehensive technical controls facilitate compliance with U.S. 21 CFR Part 11 regulations for electronic records, electronic signatures, audit trails, and data/system/user traceability
  • Connection to a central database lets you create, validate, and deploy testing methods, which can be easily transferred to other instruments and other sites around the world
  • Gives you the ability to access and perform secondary analysis on existing data sets for tests like spray pattern, plume geometry, plume velocity, evaporation rate, force to actuate, etc.
  • Comprehensive reporting functionality automatically generates submission-ready data for ANDA applications, quality audits and other regulatory submissions
  • Biopharmaceutical and Biotechnology
  • Education & Academics
  • Medical
  • Pharmaceutical
Proveris Scientific

To help our customers bring optimally-performing orally inhaled and nasal drug products to patients around the world.

Proveris Scientific Corporation delivers innovative testing platforms, laboratory services, and deep product knowledge to customers who develop, manufacture or test orally inhaled and nasal drug products (OINDPs).

Our worldwide customer base includes the top innovator and generic pharmaceutical companies, device manufacturers, CDO/CRO/CMOs, and regulatory agencies.

By understanding the critical quality attributes affecting the performance of OINDPs, and effectively controlling them from a testing and patient usability perspective, our expert team of engineers, scientists, and service professionals can help you:

  • Ensure successful product development, and prevent late-stage development failures
  • Realize significant savings in time and resources by streamlining testing workflows and eliminating manual processes
  • Evaluate the suitability of various OINDP delivery devices for compound and optimize device parameters for maximum efficacy
  • Eliminate testing variables to maintain batch-to-batch reproducibility, simplifying regulatory submissions
[Viota® software]