Skip to main content
This page is displayed using automated translation. View in US English instead?

FL-eLogbook for GMP-compliant documentation is powered by RETEL Neuhausen

Modular automation and digitalization as a full service:<br/>We stand for comprehensive solutions in automation and digitalization. Our high level of expertise is based on 50 years of experience in the cleanroom / GMP environment. <br/> <br/>Maximising your benefits: With us as your automation / digitalisation partner. From planning to operation, everything from a single source.

Why Digital logbook for efficient, reliable data?

Our electronic logbook replaces handwritten entries with a digital, tamper-proof solution that is fully GMP-compliant. Processes are documented in a more efficient, more traceable way that is ready for audit at all times. The FL-eLogbook can be optimally adapted to the needs of the customer.

Scientist using computer in laboratory

Benefits

  • Compliance: GMP-compliant recording, visualisation and automation of logbooks. FDA 21 CFR Part 11/EU Annex 11. ALCOA+ data integrityALCOA+ data integrity Repeatedly qualified and audited.
  • Efficiency and investment protection: Correct aggregation and presentation of logbook entries allows for efficient processing. Digital data capture saves human resources while increasing data quality and reliability. Replacing paper-based workflows is essential for real digital transformation.
  • Integrated and intuitive: Complete integration into the customer's system landscape. Data exchange with higher-level systems (ERP, MES, data historian, etc.). User-friendly, simple, and intuitive. Customised and reusable.

Featured Capabilities

Real-World Applications

Select...

Digitize the logbooks

Our electronic logbook replaces handwritten entries with a digital, audit-secure, fully GMP-compliant solution. It makes processes more efficient, transparent, and always audit-ready. FL-eLogbook can be tailored precisely to each customer’s needs.