21 cfr part 11 compliance capability

glp compliance facilitates the conduct of studies, promotes their full and accurate reporting, and guarantees data integrity.

All emka TECHNOLOGIES software is 100% compatible with GLP requirements for strict toxicology, safety pharmacology, and general pharmacology applications. They also provide you with an easy and reliable solution for a 21 cfr part 11-compliant environment.

software features include:

data integrity and accountability

electronic signature

usersMANAGEMENT software to define users' access rights levels,
login & passwords, validity etc.

auditSERVER to trace all actions done on the set-up in an encrypted file

audit-viewer to quickly review audit-trail lines

Microsoft Excel® macro to export, filter and check the audit-trail files

direct link for secure data transfer to your in-house database or LIMS

emka TECHNOLOGIES features on the list of vendors of 21 cfr part 11-compliant solutions of www.21cfrpart11.com