Opens in a new tab

Pernille Vestberg

Biography

Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco

From paper printouts to controlled digital records

Adam Smith
Compliance expert

Many regulated production and laboratory environments still rely on equipment that produces paper, thermal, matrix or laser printouts. The equipment may work well. The process may be familiar. But the documentation flow around the equipment can create unnecessary risk.

Paper printouts are easy to lose, damage, misread or archive incorrectly. They often need to be scanned manually, renamed manually and stored manually. In some cases, the information also needs to be typed into another system, creating more work and more opportunities for error.

The challenge is that replacing the original equipment is not always practical. It may be validated, integrated into production or expensive to change. For that reason, the smarter approach is often to modernise the documentation flow around the equipment rather than replacing the equipment itself.

A paper-to-digital record workflow captures the print output and stores it as a controlled digital file. The equipment can continue to behave as if it is printing, while the output is converted into a human-readable document and saved to a controlled location.

This creates a more reliable record process. Printouts can be stored directly as PDF or PDF/A records. Metadata such as batch number, sample ID, date, time or page information can be added. In some setups, machine-readable text can also be extracted and used in other systems.

The benefit is not only less paper. The real benefit is better control.

Records become easier to find, easier to review and easier to include in batch documentation, audit trails or long-term archives. Teams also reduce the manual work involved in scanning, naming, checking and moving documents.

For regulated environments, this is a practical way to bridge old equipment and modern documentation requirements without forcing unnecessary changes to the validated process.