“One of the most important regulatory issues is the electronic signature. In the paper notebooks, it was very difficult to track and monitor the signatures. Today, with Bookitlab ELN ,I can easily ensure that all trials are signed according to the 21 CFR part 11 FDA guidelines. The ability to use BookitLab ELN as a solution for quality control creates a significant tool to manage information and knowledge in the bioincubators. Unequivocally, I would recommend a Biotech company to use Bookitlab ELN. It helps in the documentation, ordering and ease of access to submission to regulatory authorities and most importantly, provides a prompt support and excellent customer service for any problem.”