Difference between revisions of "Document (RPS)"
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Revision as of 17:11, 19 September 2008
This is a Glossary page.
This page is under discussion and definitions and aligmnent with the BRIDG model have not yet been finalized
R1 Working Definition
Content, typically a file, be it PDF or other data, provided as part of a Submission Unit.
A collection (physical or logical) of data with the following characteristics: 1) Stewardship, 2) Potential for authentication, 3) Wholeness, 4) Human readability, 5) Persistence, 6) Global vs local context (the person that signs it is the author of all sections unless otherwise noted).
For example, regulatory processes require the submission of documents from the Applicant to the Regulatory Authority. These documents are varied in focus and are often defined by the field of study or by the regulatory application requirements of the region or Regulatory Authority (e.g., Integrated Summary of Safety, Pharmacokinetics Written Summary).
For example, Adverse Event Report, Expedited Adverse Event Report, IRB Report, X-Ray Report, Lab Summary Report, Autopsy Report, etc.
NOTE: This class is an abstract concept that contains attributes common to all types of study documents.