eCTD Viewer and Validator

GECCO is a new eCTD Viewer that provides a uniform and consistent view of eCTDs in the different regions. 

It is a compact program (< 2 MB) which runs on Windows 2000 and XP. There is no server component – eCTD folders and files simply need to be accessible to the user’s PC.The GECCO eCTD viewer/validator was designed by leading experts who were instrumental in developing the ICH eCTD specification.

GECCO can load and display an eCTD with any number of sequences (Standard and Pro editions). Simple to install (one single executable), easy to use (no training required) and with no server setup required, you can download GECCO Basic (FREE) and get started in minutes (online registration required).

The eCTD validator (GECCO Pro only) allows you to check any eCTD for compliance with the ICH eCTD specification (Version 3.2)  and regional requirements in the US, EU and Canada. Rules are user configurable (rules which are considered “critical” are always run).

GECCO can load and display an eCTD with any number of sequences (Standard and Pro editions). Simple to install (one single executable), easy to use (no training required) and with no server setup required, you can download GECCO Basic (FREE) and get started in minutes (online registration required).

The eCTD validator (GECCO Pro only) allows you to check any eCTD for compliance with the ICH eCTD specification (Version 3.2)  and regional requirements in the US, EU and Canada. Rules are user configurable (rules which are considered “critical” are always run).

Try GECCO today – www.ectd-gecco.com

GECCO is a product of ING America, Inc., USA.  ING America provides electronic regulatory submission services to the pharmaceutical industry. Services include eCTD Readiness Review, RFP preparation and assistance with selection of service and tool vendors.

Together with its sister company, ING Corporation, Tokyo, and partners in Europe, ING America is uniquely qualified to help your company get started with eCTD submissions.

www.ingamerica.com

• Valuing Pharmaceutical Innovation (14/10/2008)
• Schering-Plough Corporation (09/10/2008)
• Chugai Pharmaceutical Co. Ltd (07/10/2008)

• Nanotubes (11/06/2008)
• Readability (QRD) Testing (04/06/2007)

• Paediatric Medicines (26/01/2007)
• API Audit (14/11/2006)
• DMF project (03/01/2006)
• Data Exclusivity (29/12/2005)
• New CADREAC (16/12/2005)

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