The phrase "approval documentation" is correct and usable in written English.
It can be used when referring to the documents required to obtain approval for a project, process, or decision.
Example: "Before we can proceed with the project, we need to gather all the necessary approval documentation."
Alternatives: "authorization paperwork" or "consent documents".
The requesting department is responsible for maintaining records of approval documentation.
It is best to begin this process as early as possible so that the approval documentation can be turned in with the proposal.
All approval documentation from the IRB/IEC was retained in the respective Investigator's file and submitted to MDA.
Indeed, the FDA considers all noninvasive sensing technologies to be high-risk medical devices, and premarket approval documentation will be required for commercialization in the U.S. (165).
11 This research will investigate this in two ways: content analysis of the inclusion of 'health' in a sample of publicly available NSW EA and major project approvals documentation between 2010 and 2018 to identify the extent to which health is considered and whether this has increased over the last decade, and up to six cases of NSW EAs and project approvals.
A stringent quality controlled system with a bespoke Vacuum Vessel Project Lifecycle Management system to control the information flow, based on ENOVIA SmarTeam, was developed to handle the storage and approval of Documentation including links to the F4E Vacuum Vessel system and ITER International Organization System interfaces.
All discounts or special sanctions now need a written approval and documentation because unfulfilled verbal commitments by the sales team had created distrust amongst distributors and channel partners.
Human subjects approval and documentation of consent for NHANES III child participants was obtained through the National Center for Health Statistics Internal Review Board.
Adaptations had to be made for routine tasks such as requests, approval, and documentation of medication refills and changes outside of scheduled doctor visits.
In addition, the EU Directive for Clinical Trials was translated into UK Law in 2004 and resulted in trials of medicinal products taking longer to open as a result of increased regulatory approvals and documentation and uncertainty about different elements of its implementation (Hearn and Sullivan, 2007).
Ethical approval allowed the documentation of visual diagnosis (if available) for excluded patients but not the documentation of full visual data.
