Bioprocess platform eve®
Bioprocess platform eve®
eve® can do much more than just plan, control and analyze your bioprocesses. The software eve® integrates workflows, instruments, bioprocess information and big data in a web-based platform that allows you to organize your projects. In this way, you get an overview of your projects and can effectively implement them thanks to extensive monitoring and analysis capabilities.
The software is ready for big data and comprehensive management of bio processes.
- Planning, control and analysis
- Integrated workflows, devices and bioprocess knowledge
- Web-based project organization
- Communication via the latest OPC UA standard
- Synchronization of process-related events such as sampling and inoculation
Construction
The program consists of two parts; Core, which is the basic program itself, as well as different packages that add extra possibilities depending on which one you choose.
The packages are gradually developed depending on the wishes and requirements of customers and there is a long pipeline of planned packages.
Software package
eve® is as useful for researchers as it is for users in industry. Tailor eve® to your exact needs by combining the software packages as you wish. Choose the features that make your life easier: outline bioprocess strategies in a dizzyingly simple way – you’re just a few clicks away. Get more information via soft sensors and use DoE methods for faster results. It is up to you how you want to work with eve®. Add new features whenever you want.
The following packages are already in place:
Plan & Control
Get more information about your bioprocesses and easily design complex batch strategies in just a few steps.
- Up to 99 batches simultaneously
- Quick planning with recipes
- Batch strategies that simplify control and planning
- User Management & Reporting
Track and document everything that happens in your bio process.
- 5 predefined user roles
- Computer-based access control (IP)
- Automatic logout and password renewal
- Meets the technical requirements of FDA 21 CFR Part 11
- Report planned experiments and/or batches with all information
- Customized reports of completed batches and experiments
- Complete audit trail logs
The following packages coming soon:
GxP
Validation documentation for eve® in accordance with GMP requirements for computer-assisted processes. meets all technical requirements for FDA 21 CFR Part 11 and EudraLex Annex 11. INFORS HT offers two packages for this:
Basic
- FDA declaration of conformity
- EMA declaration of conformity
- FS (functional specifications)
- IQ (installation qualification) protocol
Plus (Q1/2018)
- FDA declaration of conformity
- EMA declaration of conformity
- FS (functional specifications)
- IQ (installation qualification) protocol
- Validation master plan
- Risk analysis
- OQ (Operational Qualification) test protocol
DoE
The first “Design of Experiment” tool designed for biotechnology thinking.
Installation
eve® is installed on a computer/server that is connected to the device(s) to be controlled. It can then be accessed from any other computer via a web browser, provided that this computer is found on the same network.
System requirements
Processor: Multicore 64-bit (Intel i5 and higher)
Memory: 8 Gb
Hard disk: HDD 250 GB (SSD 512 Gb recommended)
Resolution: 1024 x 768 (1920 x 1080 recommended)
Network: LAN adapter
Operating System: (64-bit) Windows 7 Pro, Windows 8.1 Pro, Windows 10 Pro, for multi-user access: Windows Server R2
Recommended browsers: IE11, Edge, Chrome
Annika Garnås
