#eprotocol

Our IACUC consistence module encourages the audit and observing of each examination convention including creatures, both USDA species and something else.

Highlights:

Exhaustive Review: Animal research needs to agree to USDA guidelines and authoritative strategies for the consideration and utilization of creatures. Our item encourages head specialists to make and submit definite convention applications for endorsement from the IACUC Committee.

Convention Amendments:

Research approach frequently develops over the span of an examination study. Head Investigators can then rapidly add a correction to their endorsed convention and get acknowledgment from the IACUC Committee. This streamlined procedure limits interference to the progressing research.

iacuc compliance software

Record Version Control:

A primary specialist may adjust the convention application a few times dependent on the criticism from the IACUC Committee or change in look into system. The application keeps up a background marked by totally submitted forms of the convention application with the goal that the exploration organizers can get to any emphasis for reference.

irb regulations

Joining with Other Modules:

The IACUC convention consistence module can be coordinated with other eProtocol modules, for example, IBC, SCRO, RSC, CSC, and CS. Past consistence, we additionally bolster the creature examine process with our Facility Management (LARS) and Lab Animal Health Program (LAHS) modules.img

Key Solutions eProtocol IRB system automates the management of research with human subjects. The entire application process – including development, submission etc. Key Solutions’ eProtocol IRB system automates the management of research with human subjects. The entire application process – including development, submission, tracking, review, approval, audit, and so on – is performed in a streamlined, paperless format, providing flexibility and ensuring error-free compliance with regulations.

Key Solutions offers Post-Approval Monitoring which facilitates regular inspection of protocols and enables immediate correction if required.

After the approval of a protocol, an organization needs to continuously monitor its activities to confirm that they are in line with the compliance application. If there are any discrepancies, the inspection team should either prescribe corrective action or, in extreme cases, suspend the research protocol. Our PAM module streamlines this entire process.