.csv file — one row per time point, one column per process parameter, with a batch ID column and a timestamp columnThat’s it. No software to install if you’re using the hosted version.
After logging in, click New Project. Give it a name that makes sense to your team (e.g. “Fermentation Line A — Q1 2026”) and optionally add a description.
Projects are your containers. Each project holds its own uploads, analysis runs, and reports. You can invite other team members to a project without giving them access to your other projects.
Click Upload Data and drag in your CSV file. SPECTRA will:
Once confirmed, your data is validated and ready for analysis.
Tips for your CSV:
Navigate to the Analysis tab and pick a module:
| Module | Best first question to answer |
|---|---|
| Batch Profiling (BPO) | Which batches had unusually high or low measurements? |
| Quality Attribute Analysis (QAA) | Is my process capable, and what is the risk for out-of-specifications? |
| Batch Level Modelling (BLM) | Which parameters should I select to monitor and control my process to achieve improvement? |
| Batch Comparison (BCT) | Which batches and parameters should be selected as golden batches for process monitoring and control? |
| Process Parameter Analysis (PPA) | Which control limits should I define to improve my process? |
Most teams start with BPO to get a feel for the data, then move to BLM to understand which process parameters and attributes impact outcomes (yield, defects, content, purity, etc.). After identifying significant process parameters through BLM, teams move to the BCT module to understand which batches differ and to select golden batches. These are then used in the PPA module to define and refine control limits. The QAA module is used to assess process capability and the risk of out-of-specification results both before and after control limits are implemented.
As you work through each analysis, click Add to Report on any chart that tells part of your story. When you’re ready:
The exported report includes a cover page, table of contents, and page numbers. It is ready for inclusion in a process validation file or deviation investigation package after an electronic signature by the author and reviewers in the documentation system in your environment.
Go to Project Settings → Members to invite colleagues. You can assign each person a role: