Reference lists are used throughout eReg to drive the choices that users see when they are filling out information in the system. For example, the Section Name reference list contains the names of all of the sections users can choose from when creating a regulatory template or a protocol outline, while the Lab Regulatory Item Type reference list includes all of the options that users can choose from when adding regulatory tracking items to organizations that are defined as laboratories. Read more
This course is intended for the core eReg implementation team. Read more
The purpose of this eLearning is to review the following items within Advarra eReg. Create an Organization Record Import Organization Records Edit an Organization Record Associate Contacts with an Organization If you are currently using OnCore 15, you will most likely be familiar with Organizations within eReg as the functionality is very similar between the two applications. Read more
The purpose of this module is to review the following items within Advarra eReg. Create a Template Add information about Staff and Organizations Add Additional Sections and Requirements Rearrange Sections Update a Template Status Use of Save As to Create a Template Read more
Advarra eReg stores all essential protocol documents and manages workflows while improving 21 CFR Part 11 compliance throughout your organization. The system saves staff time with efficient document routing, electronic signature notifications, and a templated approach to creating new electronic binders that’s ideal for organizations with a large number of protocols and staff. Read more
This course reviews how to manage and add documents and URLs to eReg at the organization, contact, and protocol levels. Once added, documents can be electronically signed using eReg. Read more
Shopping Cart
Your cart is empty