The situation

• Monitoring quality parameters generates data that must be collected, transmitted, interpreted and documented.

• Each partial step has its own sources of error, especially when there is media discontinuity and human interaction.

The risks

When reading and documenting manually, these problems frequently occur:

• Reading errors

• Wrong conclusions

• Forgotten signatures

• Intentional false entries

The solution

• testo Saveris 1 seamlessly automates these critical work steps.

• This minimizes sources of error and reduces risks.

• Important in a pharmaceutical environment: A recommendation from the World Health Organization (WHO) states that to ensure data integrity, modern technology should be used to minimize risks.