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U.S. FDA
U.S. FDA
The following table outlines eCTD-focused guidance documents issued by the U.S. FDA:
FDA eCTD Guidance Documents
Document
Issue Date
URL
Guidance for Industry: Providing Regulatory Submissions in Electronic Format — Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications
Rev 2, June 2008
http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm072349.pdf
The eCTD Backbone Files Specification for Module 1
2.0 June 2012
http://www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/UCM163552.pdf
ICH eCTD Specification
3.2.2, July 2008
http://www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/UCM163556.pdf
Comprehensive Table of Contents Headings and Hierarchy
2.0 June 2012
http://www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/UCM163175.pdf
FDA Implementation of Study Tagging File v2.2
2.6.1, June 2008
No longer posted - FDA web site now points to
ICH STF 2.6.1.
Providing Regulatory Submissions in Electronic Format - General Considerations
Rev 1, Oct 2003
http://www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm124751.pdf
Providing Regulatory Submissions in Electronic Format — Receipt Date
June 2007
http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm072385.pdf
Specifications for eCTD Validation Criteria
Mar 2008
http://www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/UCM163563.pdf
Portable Document Format Specifications
3.1, Jan 2012
http://www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/UCM163565.pdf
Study Data Specifications
July 2012
http://www.fda.gov/downloads/ForIndustry/DataStandards/StudyDataStandards/UCM312964.pdf
Guidance for Industry: Integrated Summaries of Effectiveness and Safety: Location Within the Common Technical Document
Apr 2009
http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM136174.pdf
Guidances
U.S. FDA
EMA Guidances
Health Canada Guidances
Japan Guidances
TGA (Australia) Guidances
Swissmedic Guidances
Agency Presentations