• Keynote by PRAC: Present and Future of Pharmacovigilance
• Expedited Reporting Requirements in the Post-Authorisation Phase
• Reporting Requirements in Special Situations in the Post-Authorisation Phase
• Clinical Evaluation of Adverse Drug Reactions
• Preparation of Periodic Safety Update Reports (PSURs)

This module is aimed at individuals from the pharmaceutical industry, academia, and regulatory authorities with experience in the clinical safety/pharmacovigilance area.

Level: Intermediate.

TECHNICAL REQUIREMENTS

To test your system compatibility, please click on the link: https://diaglobal.zoom.us/test

Operating Systems

• Windows: XP 32-bit (SP3), 2003, Vista 32-bit/64-bit, Windows 7 32-bit/64-bit
• Mac OS X: 10.5, 10.6, 10.7
• Linux: 32-bit Ubuntu 10.x,11.x 32-bit Fedora 15/16, 32-bit Red Hat 5/6, 32-bit OpenSuSE 11.4

Minimum System Requirement

• Windows: Processor – Requires Sun Java 5 or higher, Recommend ActiveX be enabled for Internet Explorer
• Mac OS X: Processor – JavaScript and cookies enabled, Requires Apple Java 5 or higher, No support for Remote Access
• Linux: Processor – JavaScript and cookies enabled, Requires Apple Java 5 or higher, No support for Remote Access

Browsers

• Windows: Internet Explorer 6, 7, 8, 9, (Win7 Only), Firefox latest (32-bit), Chrome latest
• Mac OS X: Safari 4-Mar; Firefox 2/3/3.5
• Linux: Mozilla 1.7, Firefox 2/3/3.5

Internet Connection Speed

• Windows: Intel or AMD processor (1GHz or faster), At least 512 MB RAM (at least 2 GB RAM for Vista)
• Mac OS X: Intel processor, At least 512 MB RAM
• Linux: At least 512 MB RAM

Display

• 800x600 pixel resolution or greater (1024x768 pixels recommended)