Automating data collection, processing, storage and analysis of batch records for Pharma, Life Sciences and Biotech
CPV-Auto Platform
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CPV-Auto Platform
Automating data collection, processing, storage and analysis of batch records for Pharma, Life Sciences and Biotech
At a glance
A significant portion of data used in pharmaceutical and biopharmaceutical industries continues to be found in paper-based systems that impede the efficient handling and processing of data.
The CPV-Auto platform automates the processing of unstructured data into structured, actional data and makes it accessible to teams to speed investigation and analysis.
What
CPV-Auto platform is a cloud-based service that automates the process of data collection by digitizing scanned paper-based records into a secure, GXP-compliant, structured, actionable data store. The platform facilitates easy access to Critical Production Parameter (CPP) data with search capabilities that speed analysis and decision making.
Technology
Advanced technologies, including Artificial Intelligence, Natural Language Processing, underpin the platform to rapidly process and analyze vast amounts of unstructured data mapping to fit your workflows, CPP and (Critical Quality Attributes (CQA).
Application
The platform is designed to provide a secure environment to automate data collection, processing storage, and analysis of unstructured data at speed including process conformance for reduced time to PPQ, IND, BLA, NDA filings and faster batch QC and investigation.
A significant portion of data used in pharmaceutical and biopharmaceutical industries continues to be found in paper-based systems that impede the efficient handling and processing of data.
The CPV-Auto platform automates the processing of unstructured data into structured, actional data and makes it accessible to teams to speed investigation and analysis.
Business Impact
Handles diverse data structures and workflows
Converts unstructured data into structured insights– to support data-driven decision-making.
User friendly Search for non technical staff
Speeds investigation, analysis and comparison– for faster batch QC and reduced time to PPQ, IND, BLA, and NDA filings.
Features Real-Time CPP Monitoring
Faster data processing– over traditional methods to make informed decisions for operational efficiency.
Compliant with 21CFR Part 11 and GAMP 5
Ensures electronic records are equivalent to originals, secures access, tracks activity, and maintains audit trails.
CPV- Auto Platform Case Studies
Biopharmaceutical manufacturer realizes 80% reduction in search and analysis time
Ingesting unstructured data from various stages of engineering and bio-manufacturing, using the CPV-Auto platform, this research company realized faster, easy access to data (stored in their data warehouse) for both analysis and comparison. The structured data obtained, using the platform’s AI-assisted conversion empowered the company to more easily make informed decisions, drive operational efficiency, ultimately transforming their manufacturing operations.Read More
Monoclonal antibody company gains new insights into mAB characterization
Ingesting and merging structured and unstructured data from numerous runs, cycles, and lots using the CPV-Auto platform, this company streamlined analysis, enabling the manufacturing team to quickly identify outliers for early intervention. Read More
CPV- Auto Platform Implementation
Tailored to fit your requirements during our structured implementation process.
Identify workflows and document types.
Automate text extraction, identify attributes regardless of layout.
Classify documents with workflow identify key parameters.
Validate data accuracy via internal peer review.
Perform quality reviews to ensure security, integrity and reliability of data and workflows
Trial Stage: Identify your unique needs and deliver a Proof of Value (2-4 weeks)
During the trial stage, we collaborate with you to review Critical Production Parameters (CPP) and Critical Quality Attributes (CQA), identify sample documents, and create custom templates. This process aims to:
- Demonstrate the value of the CPV-Auto solution for your organization.
- Gather all requirements and document operational expectations, including Service Level Agreements (SLAs).
Over 2-4 weeks, Aventior will process sample documents (e.g., records, handwritten notes, certificates) from your approved file-sharing platform (e.g., SharePoint, Box). Once you validate the data, we will proceed to refine document parameters and workflows.
By the end of the trial, you’ll gain a clear understanding of how CPV-Auto operates before moving to the Production Stage.
Operational Stage: Expand production volume, set up customer access module for visabiliy (4-6 weeks)
As we move to production, larger data volumes are processed (ensuring that customizations made to fit your data and workflow needs).
In this stage, which lasts between 4-6 weeks, we work with you to ensure that CPV-Auto seamlessly integrates into your workflow, processes data at scale and delivers the expected data insights.
Production Stage: Deploy full production volume at scale, confirm quality (1-2 weeks)
Full Operation Stage. After passing production, we deploy the Customer Access Module to give you control and visibility over your data. The module includes real-time access to all digitized records including advanced search, audit logs, as well as performance data and reporting tools.
Technical and Program Support is provided across the stages to ensure your solution meets expectations.
Transform Paper Documents Into Digital Insights.
