Negotiations and Award

Safety Reviewer

Guidelines

Overview

The purpose of the Safety Reviewer Guidelines is to provide Organization Subprocess Formualation instructions for the role of Safety Reviewer. These Guidelines are divided into areas based on the class of activities: Administrative Tools, Register Key Players, Develop Program-Wide Model Drugs and Medications, Develop Field Center-Wide Model Drugs and Medications, Drugs and Medications & Deliverables Negotiations, and Analysis.

Organization: ORG

Guidelines

  1. Administrative Tools
  2. Register Key Players
  3. Develop Program-Wide Model Drugs and Medications
  4. Develop Field Center-Wide Model Drugs and Medications
  5. Drugs and Medications & Deliverables Negotiations
  6. Analysis

Subprocess

1 Administrative Tools

-Administrative Tools-
 Register
 Login 
 Change Password    
 Forgot UserID/Password 
 Frequently Asked Questions (FAQs)
 Print Instructions 
 Regulations and References

2 Register Key Players

3 Develop Program-Wide Model Drugs and Medications

4 Develop Field Center-Wide Model Drugs and Medications

5 Drugs and Medications & Deliverables Negotiations

 Awardee:
  Review Drugs and Medications    
  Electronically Approve Drugs and Medications

6 Analysis

 Report Tools

Implementation:

Mockup (html)
Implementation (html)

Contacts:

Name- Phone-Email (mailto-hyperlink)

References:

Title- Author- Library (html)