It’s here, and it’s our best release yet!
We’re excited to announce the next major iteration to QbDVision. Designed and validated top to bottom to bring you the latest tools to advance your pharmaceutical manufacturing activities.
Keep reading to find out more, or try it today.
Intelligent Processing of Materials
Do you have a filing cabinet full of Certificate of Analysis records? Have you experienced an out-of-specification event due to an irregularity in material specifications? Are you getting lot data from suppliers that are unharnessed?
Our new, AI-based CoA Import feature provides an automated workflow for raw material management that changes the way you work with this type of data, including:
- Automated data extraction of material attribute data from paper/electronic CoAs
- Storage of results data in QbDVision via a Review-by-Exception methodology
- Logging of lot information in the material record
- Auto-detection of outliers in the data for any attribute relative to previous lots
Process Development, Simplified
We’ve completely redesigned Process Explorer to make it easier and faster to use. Explore your process in a dynamic, tree-like view and see your process and data, side-by-side and quickly make edits to drafts inline while viewing your process inputs and outputs.
Additionally, we’ve added flexibility to our process modeling. Process components and materials can now be shared across unit operations, allowing you to use the same piece of equipment in multiple steps in your process. And, our new process level definitions allow you to model common parameters across all your unit operations, like site humidity, temperature, and other utilities specifications, making it even easier to build out your process.
Do More with Your Teams
QbDVision has a new homepage experience that brings the data across your projects to life. When first logging in, you now see at a glance all the activity and action items you need to know. This new view provides a rich set of insights that help you take action on critical alerts, as well as get a sense of how your broader team is progressing.
As part of this release, we are introducing a new, simplified module for document and employee training management. It’s the first of its kind in our industry and designed to automate compliance for small and early-stage companies. We have seen that many companies are still using paper records for training because of the prohibitively high cost of large-scale commercial systems. QbDVision now gives you access to 21 CFR Part 11 compliant document management at a fraction of the cost of standard eQMS solutions. It also lets you manage and capture basic training requirements. Teams can define individual training plans and curricula that are assigned, managed, and tracked through the platform. Experiencing the value of digital training has never been easier!
And so much more
Automatic generation of a comprehensive QTPP report that aggregates many aspects of our prior reporting elements in one comprehensive package.
An automated FMEA report that assembles before-and-after risk information by unit operation, based on one of our most popular views.
Automatic generation of a risk management plan document that helps customers rapidly generate and approve RMPs and avoid time wasted manually drafting these documents.
We also made several customer-driven enhancements to other reports including our risk map and process flow maps.
This new validated version boasts mature features to support knowledge and quality risk management. So, whether you’re in process development, scale-up activities, or process validation, QbDVision can help accelerate your timelines, improve collaboration and visibility, and reduce development costs advancing your program toward successful registration.