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 ofwww.21cfrpart11.com