Aris Global
Top Menu

Webcast Registration

Hosted Solutions for Safety and Regulatory Tracking: Gain Control While Removing the Cost & Complexity



Register for a complimentary, 45-minute Aris Global® webcasts that effectively showcase new and improved hosted software solutions for safety & pharmacovigilance and regulatory tracking. Learn how you can prepare for the FDAAA Electronic reporting initiative.


Yes, please register me for the following webcasts:

Hosted Drug Safety & Outsourced Case Processing: Your One-Stop, Cost-Effective Solution for Achieving Safety Control - February 4, 2010 - 10:00 EST / 15:00 UTC / 16:00 CET

Hosted Drug Safety: Removing the Barriers of Cost, Complexity & Constraints - February 11, 2010 - 14:00 EST / 19:00 UTC / 20:00 CEST

Hosted Drug Safety & Outsourced Case Processing: Your One-Stop, Cost-Effective Solution for Achieving Safety Control - February 18, 2010 - 14:00 EST / 19:00 UTC / 20:00 CEST

Hosted Regulatory Tracking: Managing Regulatory Obligations with Greater Speed and Efficiency - March 2, 2010 - 10:00 EST / 15:00 UTC / 16:00 CET

Preparing for FDA Mandatory Electronic Reporting - March 4, 2010 - 10:00 EST / 15:00 UTC / 16:00 CET

Preparing for FDA Mandatory Electronic Reporting - March 23, 2010 - 14:00 EDT / 19:00 UTC / 20:00 CET

Hosted Regulatory Tracking: Managing Regulatory Obligations with Greater Speed and Efficiency - March 24, 2010 - 14:00 EDT / 18:00 UTC / 19:00 CET

Hosted Drug Safety & Outsourced Case Processing: Your One-Stop, Cost-Effective Solution for Achieving Safety Control - March 25, 2010 - 10:00 EDT / 14:00 UTC / 15:00 CET

Please send me the archived link for on-demand viewing.
Please send me the detailed white paper, "agOnDemand: Removing the Barriers to Total Safety".


Contact Information
All bold fields are required. Only those with valid business addresses will be registered. Aris Global reserves the right to refuse registrations from individuals we consider competitors.

Remember Me (What's this?)

Describe your role:

Pharmacovigilance / drug safety
Clinical research / operations
Central / Clinical IT
Regulatory Affairs
Medical Information
CRO
Other

What stage of drug development are you currently at?


Approximately how many AEs do you process each year?


How did you hear about this webcast?


Support Login Contact Aris Global Terms Careers Privacy Policy Site Map