Key Benefits
The CPV-Auto™ platform provides a secure environment to automate the process of data collection, processing, storage, and analysis. The digitally scanned documents - (Batch Records, Certificates of Analysis, Viral Vector Clearance Documents, Quality Control Forms, Donor Charts, Instrument Print Outs, and others) are processed through the CPV-Auto™ platform, curated, and the final structured data is extracted and uploaded into the client systems eliminating / reducing the need for technical support.
The platform was designed to empower Pharma and Biotech MSAT, CMC, QA and Production teams to process unstructured data at speed.
These are the key benefits realized:
Quicker time to market
Driven by faster analytics and data visibility facilitates quicker decision making and time to market
Improved mandatory data and audit readiness
Being a 21 CFR Part 11 compliant system, ensures complete traceability and privacy of data along with improved and accessible data for reduced errors
Process conformance - improved time to PPQ, IND, BLA, NDA filings
Allows improved visibility on all process parameters, leading to faster decision making and compliance
Reduced costs & faster batch releases
Reduced manpower costs, for data entry and validation coupled with reduced errors and a quicker turn around time ensures faster QC of batch releases
Faster QC and batch records
Improves efficiency and facilitates faster decision making
Data availability and consolidation for MSAT
Automated processes improve data availability and consolidation that goes to MSAT for analysis