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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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How You Can Automate Batch Release in APQR?

Automate Batch Release with APQR to cut errors, speed up timelines, and ensure compliance with a smart, real-time checklist for pharma QA.
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AmpleLogic’s Role in Future Trends in Quality Management Systems (QMS)

Pharmaceutical companies and medical device manufacturers are racing to ditch outdated paper trails for cutting-edge, AI-powered quality management systems.
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AL Ideathon 2025 - Reshaping Life Sciences operations! - Amplelogic

The AL Ideathon – Reshaping Life Sciences’ operations is an industry-leading innovation challenge designed to address critical challenges within the life science industry.
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Pharma IT Cost Reduction Strategies That Save 70%

Discover pharma IT cost optimization strategies. Save 70% on eQMS and achieve compliance at lesser cost without sacrificing performance or control.
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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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How is Sterile LIMS Different from OSD LIMS

Discover how AmpleLogic Sterile LIMS helps pharmaceutical companies streamline sterility testing, ensure data integrity, and maintain full compliance with FDA and GMP standards.
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Human Error Data Integrity in Pharma

Learn how to reduce human-error risks and ensure data integrity in pharma with FDA, MHRA, WHO, and PIC/S-compliant controls using AmpleLogic.
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Investigation of OOS Results in Analytical Testing

OOS results occur when lab tests fall outside approved limits. Proper investigation ensures whether it s an analytical error or a true product-quality issue.
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