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ELOG is a Web application written by Stefan Ritt in C which can be used to create personal and common logbooks. It has been developed at the Paul Scherrer Institute originally for shift logbooks in the particle physics experiment MEG, but is now widely used in other fields. -- Wikipedia

6 Digital Tools That Reduce Human Errors in Lifesciences

Anyone who has sat through a regulatory audit knows how quickly small mistakes build up. A missing training record raises questions about broader compliance.
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AmpleLogic eLogbook | Electronic Logbook Software for Pharma

Elevate your lab operations with the Best Electronic LogBook Software. Experience efficiency and innovation with AmpleLogic eLogbook.
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Understanding the GMP Logbook Requirements - Amplelogic

Discover the essentials of complying with GMP logbook requirements in this comprehensive guide. Gain insights into the importance of accurate record-keeping
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7 Common Compliance Issues Faced by the Pharmaceutical Industry

The pharmaceutical industry is critical in safeguarding public health by researching, developing, and manufacturing life-saving drugs.
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Top 7 Queries Addressed: Data Integrity and CGMP Compliance

This article provides a clear insight into the significance of data integrity within the framework of current good manufacturing practice
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Compliance Document Management System for Lifesciences

AmpleLogic’s document management system exemplifies this by integrating AI along with advanced features such as electronic signatures, version control, and automated workflows to meet global standards while streamlining
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Best Electronic Batch Manufacturing Record (EBMR) Software

Optimize pharmaceutical manufacturing with AmpleLogic Electronic Batch Manufacturing Record (EBMR) Software for compliance, efficiency, and digitization.
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HIPAA

HIPAA, enacted in 1996, is the U.S. law ensuring data privacy and security in healthcare through strict regulatory standards.
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How Human Error Fuels Cybersecurity Risks in Life Sciences

A single misstep in logging production data. A forgotten password at a manufacturing terminal. An unsecured device connected to the shop floor.
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What is a 21 CFR Part 11 Compliant Document Management System?

Discover how a 21 CFR Part 11 compliant Document Management System ensures FDA compliance, secures electronic records, and streamlines document control in regulated industries.
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