Eventbrite
Contact the organizer for event and ticket information.
GlobalSubmit Product Team
GlobalSubmit is a products and services company that provides transparency in regulated healthcare products. The U.S. Food & Drug Administration and leading life sciences companies use our flagship applications, REVIEW™ and VALIDATE™, to review and validate electronic submissions. GlobalSubmit leads international efforts, comprising industry and government agencies, to standardize product and study information. The company is headquartered in Philadelphia, Pennsylvania.
Events
eCTD Regulations and Status Worldwide (Session 2) 12/8/09 11AM - 12PM
Philadelphia | View Map
For those of you who weren't able to sign up for the November 5th event, or have colleagues that didn't hear about it in time, we're...
GlobalSubmit REVIEW™ and VALIDATE™ Open Product Demonstration 10/23/08 2PM - 3PM
Conference Call | View Map
THE Industry Standard For Review & Validation Of Global Electronic Submissions GlobalSubmit REVIEW™ and GlobalSubmit VALIDATE™ are...
GlobalSubmit's 2008 Executive Webinar Series: Mastering the eCTD - Working With Metadata 10/22/08 11AM - 12PM
Conference Call | View Map
Developing and assembling an eCTD requires a working knowledge of practical techniques associated with metadata. This seminar will...
GlobalSubmit REVIEW™ and VALIDATE™ Open Product Demonstration 10/21/08 10AM - 11AM
Conference Call | View Map
THE Industry Standard For Review & Validation Of Global Electronic Submissions GlobalSubmit REVIEW™ and GlobalSubmit VALIDATE™ are...
GlobalSubmit's 2008 Executive Webinar Series: Mastering the eCTD - Archiving Options and Best Practices 10/1/08 11AM - 12PM
Conference Call | View Map
Electronic submissions are legal records and must be properly archived to ensure integrity and authenticity of these records long term. ...
GlobalSubmit's 2008 Executive Webinar Series: Mastering the eCTD - Understanding eCTD File Formats 9/10/08 11AM - 12PM
Conference Call | View Map
Although few people still think of an eCTD as an “XML submission” anymore, many people are still unclear on acceptable file formats for...
GlobalSubmit's 2008 Executive Webinar Series: Mastering the eCTD - Understanding Regional Differences 8/20/08 11AM - 12PM
Conference Call | View Map
The eCTD is not a global application! This session will explore the differences in regional requirements for both the CTD and the eCTD,...
GlobalLinks 2008 8/14/08 8AM - 8/15/08 6PM
Las Vegas | View Map
GlobalLinks 2008 is the first inaugural user conference sponsored by GlobalSubmit. The goal of this annual meeting is to provide thought...
GlobalSubmit's 2008 Executive Webinar Series: Mastering eCTD Readiness - Scanned Input Preparation 7/23/08 11AM - 12PM
Conference Call | View Map
Scanned documents have always been a part of regulatory submissions. Although most companies strive to replace scanned documents with...
GlobalSubmit's 2008 Executive Webinar Series: Mastering the eCTD- By The Numbers 7/2/08 11AM - 12PM
Conference Call | View Map
How many eCTDs have really been submitted? What are the trends in each market? This insightful presentation gives a summary of progress...
GlobalSubmit's 2008 Executive Webinar Series: Introduction To Regulated Product Submissions (RPS) 6/10/08 11AM - 12PM
Conference Call | View Map
Many people have heard of RPS, but few are familiar with the specification and its impact. Publicly available information has been...
GlobalSubmit's 2008 Executive Webinar Series: Mastering eCTD Submission Reviewing-Current Best Practices 5/8/08 11AM - 12PM
Conference Call | View Map
Do you understand what FDA reviewers look for in reviewing your eCTD submissions? This session will focus on best practices that will...
GlobalSubmit's 2008 Executive Webinar Series: Mastering eCTD Operators 4/23/08 11AM - 12PM
Conference Call | View Map
eCTD is all about lifecycle – and lifecycle depends on proper use of eCTD operators. Learn about operators and when they should be used;...
Contact organizer:
Your message has been sent!