In the fast-paced world of biopharmaceuticals, staying ahead means staying efficient and compliant. Digitizing your paper-based records is not just a modernization step; it's a necessity for streamlined operations and adherence to regulatory standards. That's where CPV-Auto™ NXG comes in – your smart solution for biopharmaceutical record digitization.
Step 1: Seamless Conversion
CPV-Auto™ NXG simplifies the daunting task of converting paper records into digital format. With advanced features like auto text extraction and built-in categorization, this software takes the manual effort out of digitization. Say goodbye to time-consuming data entry and hello to instant, accurate results.
Step 2: Effortless Organization
Sorting through heaps of digital files can be just as challenging as dealing with paper records. CPV-Auto™ NXG's built-in categorization feature is your digital filing assistant. It classifies documents uploaded on platforms like Box Drive into their respective workflows. This means easy access, efficient processing, and a well-organized digital archive.
Step 3: Automation for Precision
Digitization often comes with the challenge of varying document layouts. CPV-Auto™ NXG solves this problem with the power of AI and ML. It automates data extraction, regardless of how your documents are structured. The result? Data accuracy that meets industry standards.
Step 4: Accurate to the Pixel
No scan is perfect, and minor shifts or skews can lead to inaccuracies in your digital records. CPV-Auto™ NXG doesn't miss a beat. It employs coordinate mapping to compensate for these shifts, ensuring that your digitized records mirror the original data down to the pixel.
Step 5: Data Integrity Assurance
Biopharmaceutical data is sensitive, and integrity is non-negotiable. CPV-Auto™ NXG lets you set range parameters, specifying the acceptable minimum and maximum values for parameters. This safeguards your data and ensures compliance with industry standards.
Step 6: Quality Control
Even with advanced technology, a human touch is invaluable. CPV-Auto™ NXG incorporates a peer review process, independently verifying data points with a human in the loop. This double-check system adds an extra layer of quality control to your digitization process.
Step 7: Security You Can Trust
Compliance with regulatory standards is paramount in biopharmaceuticals. CPV-Auto™ NXG understands this and is designed to be 21-CFR Part 11 and GAMP compliant. Your data's security is never compromised.
Ready to Transform Your Biopharmaceutical Records?
CPV-Auto™ NXG is not just software; it's a game-changer for biopharmaceutical record management. With it, you can digitize with confidence, ensuring efficiency, accuracy, and compliance at every step.
Don't let paper-based records hold you back. Embrace the future of biopharmaceutical record digitization with CPV-Auto™ NXG today.
Connect with us at https://aventior.com/unstructured-data-solutions-cpv-auto-nxg/ to learn more and experience the difference for yourself.
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