At Pharmaceutical sites, all activities should be recorded to logbooks to comply with GMP regulations. Having manual logs such as written or excel sheet logbooks are of common practice. This limits the further analysis of the logs. Maintaining the logbooks become too costly when manual methods are used and security concerns arise. - Digitize all room logs and forms capturing activities on the factory floor - Access your data easily and remotely at all times - Improve security and quality by using personal digital signatures - Comply with GMP regulations - Follow SOPs and workflows for log entry and/or logbook design changes When users leave Digital Logbook reviews, G2 also collects common questions about the day-to-day use of Digital Logbook. These questions are then answered by our community of 850k professionals. Submit your question below and join in on the G2 Discussion.

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