The phrase "authorization submission" is correct and usable in written English.
It can be used in contexts where someone is submitting a request or document for approval or permission, often in formal or administrative settings.
Example: "Please ensure that your authorization submission is completed by the end of the week to avoid any delays in processing."
Alternatives: "approval request" or "permission application".
Dr. James H. Scully Jr., chief executive of the association, said some insurers had tried to "circumvent the law" by "imposing new requirements for prior authorization and the submission of treatment plans for mental health services where there were no comparable requirements on the medical-surgical side".
The extended openEHR RM model is more semantically aligned with the concepts involved in authorization and claim submissions.
The extended model adds subclasses and an attribute to the COMPOSITION class to represent information on authorization and claim submissions.
In the third approach, the openEHR ADMIN_ENTRY is extended with classes designed for authorization and claim submissions, and an ISM_TRANSITION attribute is added to the COMPOSITION class.
The TISS standard is a set of mandatory forms and electronic messages for healthcare authorization and claim submissions among healthcare plans and providers in Brazil.
The results section presents an extension of the openEHR RM to deal with administrative authorization and claim submissions and the archetypes designed to represent the TISS standard.
For instance, new sets of clinical information to support authorizations and claims submissions are usually under discussion.
The median time between authorization and the date of submission of the first included PSUR was 6.9 (range 0.6 24.6) years.
Key requirements include having a legally mandated authority with qualified staff in place, and the capacity for review of submissions of marketing authorization, postmarketing surveillance, and lot release, as well as access to a laboratory for testing vaccines and competent staff for regulatory inspections and regulatory oversight for clinical trials [ 5– 7].
Mandatory test data submission and review, prompt feedback to sites and site authorization pending test data approval have proven very important, leading to increased and sustainable compliance with the imaging protocol [ 12, 15].
