PRODUCTS->IRB MANAGEMENT

Clinical Manager^TM IRB offers the following features¡G

Create electronic IRB submission forms and assign data validation rules to the fields.

Enable investigators to complete and submit applications electronically. The data validation rules ensure accuracy and reduce the need for re-submission.

Enable investigators to attach any type of external file or document such as the Principal Investigator C.V. or informed consent to a submission.

Enable investigators to stay on top of all their regulatory documents with an easy-to-use document tracking screen.

Manage both review committees and subcommittees, including membership meeting dates, and locations.

Track key personnel for every research study.

View lists of applications electronically submitted by investigators and assign them to review committee meetings.

Have meeting agendas automatically created for you, and adjust them as you wish. Print your agendas any time you wish.

Record minutes for every agenda item at every meeting. Print your meeting minutes any time you wish.

Enable committee members to securely log in from anywhere and review submissions (including all attached documents) right on their computer screen.

Query the database for submissions by investigator, sponsor, IRB number, date range, funding source, or any number of other custom search criteria.