QvoBatch improves quality by minimizing error potential during batch processing.
Excursion from expected operating standards are immediately flagged, allowing for real-time monitoring and attention.
With minimal needed customization, the implementation schedule for QvoBatch is shortened.
QvoBatch’s Record Builder allows for rapid development and cross-site implementation.
QvoBatch is designed to require minimal customization, saving time and money.
By designing with quality and regulatory compliance in mind, companies are assured of right-first-time electronic batch record conversion.
Designed with ease of use for production operators while maintaining compliance standards, QvoBatch enables positive change by promoting right-first-time manufacturing with real-time monitoring ability.
“A complex system that works is invariably found to have evolved from a simple system that worked. The inverse proposition also appears to be true: a complex system designed from scratch never works and cannot be made to work. You have to start over, beginning with a simple system.”
— John Gall, systems theorist
Frequently Asked Questions
What types of clients do you service?
Qvolve solutions are designed for FDA regulated batch processing companies, including finished pharmaceuticals, API, excipient, nutraceuticals and OEM medical device manufacturers and suppliers.
What is your turn around time?
EBR and electronic documentation implementation is dependent on the existing document standards and systems of the client, however Qvolve offers several standard workflows and templates designed to shorten the implementation phase.
What are the advantages of Electronic Batch Records?
EBR enables real-time monitoring of production data and the ability to reduce human error traditionally associated with data transcription. Fully complaint with CFR and GMP standards for data handling and software validation, Qvolve offers clients improved access to historical production data trends.