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GMP log book for Industry 4.0

io.Equipment– Digitize your Equipment Logs

Maximizes data integrity and documentation maturity
Intuitive and user-friendly to shop-floor teams
Digitizes your log book shelves and clipboard activities

Try io.Equipment

Simplified information and documentation solution

Digital recording of data makes information accessible and transparent at all times.

Use with cleanroom-compatible tablet computers directly at the production workstation
Keep track of all events such as production, cleaning, maintenance, breakdowns or calibration for each equipment
Simplify documentation processes, e.g. when creating one record for multiple log books
Versatile research features, e.g. for batch releases or continuous improvement

Regulatory compliance for GMP environments

io.equipment provides full GMP-compliant documentation of equipment usage as required by the FDA and the European Commission.

Replace old paper logbooks
Meet FDA and European Commission documentation requirements
Audit-proof data storage in accordance with FDA CFR 21, Part 11

Data integrity through Blockchain technology

Blockchain audit trail enables data integrity and privacy

With optional blockchain timestamping, data can be stored absolutely tamper-proof without revealing the data itself.

Full audit trail with version history for all records
Timestamping with SHA-256 hash fingerprints keeps your data private
Proven evidence of data integrity

Overview Equipment Logs

Clear presentation of all books for quick retrieval

Search function

Comprehensive search function for incidents

Blockchain extension

Next generation Audit Trail with optional Blockchain extension

Leading companies rely on Shiftconnector^® and io.Equipment

Air Liquide

eschbach was established in 2005 in southern Germany, close to Basel. Their ISO 9001 certified software development complies to GAMP5. Eschbach’s solutions are running live at companies like Roche, Sanofi, and Bayer.

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