Welcome to e-TrialDoc™

01

Superior Operating Procedures

Welcome to our e-TrialDoc SOPs ™ online directory. You can quickly find the clinical research information you need through various navigation options. You may choose to find your information through intuitive maps or tables.

Industry and government regulatory authorities often require that clinical research sites develop standard operating procedures. Based on our years of clinical trial experience, our organization has developed this e-TrialDoc™

SOPs ™ directory which covers over 100 issues pertaining to the ethical, efficient, and profitable conduct of clinical research.

02

Leads

The Leads module allows subscriber sites access to general information regarding upcoming clinical studies. These postings are provided by sponsors to alert other research sites interested in an upcoming clinical trial.

We have also developed a tool for sponsors to learn about the site capabilities of e-TrialDoc™ subscribers.

03

Communications

The internet is an ideal environment to disseminate information to groups of geographically dispersed users. This module provides a secure area to house documents specific to clinical trials and can link geographically disparate sites. Our communications module will allow sponsors to correspond electronically rather than by cumbersome and often confusing paper trails. This platform should allow better and more direct communication between the trial sponsor or clinical research associate and the clinical research site.

04

Government

This module provides information regarding site compliance with OSHA, EPA, Department of Transportation and Health and Human Resources Rules and Regulations.

05

Tracker

Development of our Trial Tracker tool will allow research sponsors to track usage by clinical research sites within protected elements of the website. The purpose for this capability is to be able to document both FDA training and user access to specific documents.

06

Tutor

This module helps sites with the challenging task of providing education and training to clinical research staff and investigators. Included are courses that train and evaluate the knowledge base of human subject testing. On request, we can also provide specific drug trial training systems to allow sponsors to assure a consistent knowledge base among participating sites.