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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 AmpleLogic eLogbook | Electronic Logbook Software for PharmaElevate your lab operations with the Best Electronic LogBook Software. Experience efficiency and innovation with AmpleLogic eLogbook.
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.
Compliance Document Management System for LifesciencesAmpleLogic’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
Understanding the GMP Logbook Requirements - AmplelogicDiscover the essentials of complying with GMP logbook requirements in this comprehensive guide. Gain insights into the importance of accurate record-keeping
7 Common Compliance Issues Faced by the Pharmaceutical IndustryThe pharmaceutical industry is critical in safeguarding public health by researching, developing, and manufacturing life-saving drugs.
Top 7 Queries Addressed: Data Integrity and CGMP ComplianceThis article provides a clear insight into the significance of data integrity within the framework of current good manufacturing practice
Best Electronic Batch Manufacturing Record (EBMR) SoftwareOptimize pharmaceutical manufacturing with AmpleLogic Electronic Batch Manufacturing Record (EBMR) Software for compliance, efficiency, and digitization.
HIPAAHIPAA, enacted in 1996, is the U.S. law ensuring data privacy and security in healthcare through strict regulatory standards.
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.
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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