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Sage Templates for eCTD - Sage Submissions

Welcome to Sage Submissions. Sage Submissions is dedicated to helping you streamline the process for creating submissions for drug, biologic and medical devices. Sage Templates , a MS Word-based tool, helps you create documents that support the global electronic Common Technical Document (eCTD) submission standard. The templates also support all FDA CDRH and Global Harmonization Task Force (GHTF) Summary Technical Documentation (STED) pre-submissions and submissions in Electronic Copy format. Want to exp...

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Sage Templates for eCTD - Sage Submissions | sagesubmissions.com Reviews

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Welcome to Sage Submissions. Sage Submissions is dedicated to helping you streamline the process for creating submissions for drug, biologic and medical devices. Sage Templates , a MS Word-based tool, helps you create documents that support the global electronic Common Technical Document (eCTD) submission standard. The templates also support all FDA CDRH and Global Harmonization Task Force (GHTF) Summary Technical Documentation (STED) pre-submissions and submissions in Electronic Copy format. Want to exp...

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Sage Templates for eCTD - Sage Submissions | sagesubmissions.com Reviews

https://sagesubmissions.com

Welcome to Sage Submissions. Sage Submissions is dedicated to helping you streamline the process for creating submissions for drug, biologic and medical devices. Sage Templates , a MS Word-based tool, helps you create documents that support the global electronic Common Technical Document (eCTD) submission standard. The templates also support all FDA CDRH and Global Harmonization Task Force (GHTF) Summary Technical Documentation (STED) pre-submissions and submissions in Electronic Copy format. Want to exp...

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Sage Templates for eCTD - Sage Submissions

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Welcome to Sage Submissions. Sage Submissions is dedicated to helping you streamline the process for creating submissions for drug, biologic and medical devices. Sage Templates , a MS Word-based tool, helps you create documents that support the global electronic Common Technical Document (eCTD) submission standard. The templates also support all FDA CDRH and Global Harmonization Task Force (GHTF) Summary Technical Documentation (STED) pre-submissions and submissions in Electronic Copy format. Want to exp...

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Sage Submissions - Sage Submissions

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Don't have an account? Regulatory Submissions - Electronic Submissions - Publishing and Document Management. Web Design and Hosting by WebWizard Works.

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515-consulting.com

September 2012 - 515 Consulting Group515 Consulting Group

http://www.515-consulting.com/2012/09

Electronic Regulatory Submission Solutions. Skip to primary content. Skip to secondary content. Monthly Archives: September 2012. DIA EDM/eSubs only 2.5 weeks away. September 20, 2012. The DIA EDM/eSubs conference, or as the DIA calls it, “EDM and ERS/eCTD 2012” , being held at the? Baltimore Hilton Hotel from? October 9-11, 2012? Tutorials: October 8), is only 2 weeks away? Find out more at http:/ www.diahome.org/en/Flagship-Meetings/12003-EDM.aspx. FDA releases new eCTD Module 1 documents.

515-consulting.com

Partners - 515 Consulting Group515 Consulting Group

http://www.515-consulting.com/partners

Electronic Regulatory Submission Solutions. Skip to primary content. Skip to secondary content. 515 Consulting Group is an authorized partner with:. 515 Consulting partners with EXTEDO as a reseller of their leading regulatory software applications including. ECTDmanager, a leading CTD/eCTD/NeeS/eCopy compilation, viewer, validator and publishing tool,. EURS, the official eCTD review and validation tool for the European Medicines Agency (EMA) and its associated countries,. US FDA CDER and CBER. In the li...

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Sage Templates for eCTD - Sage Submissions

Welcome to Sage Submissions. Sage Submissions is dedicated to helping you streamline the process for creating submissions for drug, biologic and medical devices. Sage Templates , a MS Word-based tool, helps you create documents that support the global electronic Common Technical Document (eCTD) submission standard. The templates also support all FDA CDRH and Global Harmonization Task Force (GHTF) Summary Technical Documentation (STED) pre-submissions and submissions in Electronic Copy format. Want to exp...

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