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How much does one lost experiment cost?
FermWorks manages the process data, control, analysis, and security of your experiments and production runs.
FermWorks reduces the chance of expensive, catastrophic loss of experiment data and materials. |
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FermWorks™ 2.3 |
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Reduce Risks |
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FermWorks is a robust data logging and supervisory process control application that brings unparalleled flexibility and reliability to cell culture and bacterial experiments. FermWorks currently runs in process development laboratories and pilot plants at leading pharmaceutical companies, where it is essential for protecting serious investments in pharmaceutical processes. Its automation of manual tasks helps eliminate errors and risks in the fermentation process, resulting in a higher-quality product.
Increased efficiency and repeatability, adherence to Good Laboratory Practices, FDA compliance, and data security make FermWorks a must for protecting serious investments in biopharmaceutical production processes. |
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"It costs us $100,000 to carry out a single perfusion experiment in our Process Development lab. FermWorks gives us confidence that our experiment data is secure and accessible." |
PD Lab Manager,
large west coast pharmaceutical company |
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Flexible Control Strategies
Control your Processes |
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Run standard or custom control strategies in software |
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Monitor all controllers through a common user interface |
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Define recipes for simple or sophisticated sequences of control actions |
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Real-Time Analysis
Clarify Results |
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View acquired, calculated, and off-line values together as process data |
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See live or historic process data on full-featured trend graphs |
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Annotate any part of the process using the Electronic Notebook |
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Display and export reports of process data and custom calculations |
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View step-by-step progress of recipes and experiments |
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Present results to colleagues on a live system, using a remote station |
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Secure Reliable Data Storage
Meet Data Security Requirements |
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Review history of changes to the system with the Audit Log |
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Archive process data through robust backup system |
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User Security and Management
Ensure FDA Compliance and Security |
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Comply with FDA 21 CFR Part 11 regulations |
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Conform to ASTM Committee E55 (PAT) initiative |
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Enforce authorization of selected changes by Electronic Signatures |
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Track operator, authorization, time, and settings of all changes |
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Grant fine-grained security access based on user |
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