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The FAI process usually consists of fully testing and inspecting either the first part produced by the new process or a sample from the first batch of parts. First article inspection is typically a purchase order requirement of the purchaser for the supplier to complete. If the manufacturer doesn't have the in-house capability or if the ...
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The process is analogous to 'after-market' parts for automobiles, except that the United States aircraft parts production market remains tightly regulated by the FAA. An applicant for a PMA applies for approval from the FAA. The FAA prioritizes its review of a new application based on its internal process called Project Prioritization. [5]
The Articles for creation (AfC) process is designed to assist any editor with creating a new page as a draft article, as well as submitting their draft article for review.. This process must be used by new or unregistered editors, as well as editors with a conflict of interest, since they cannot directly create a new page in Wikipedia's mainspace, where all articles resi
The TSO authorization (also called TSOA) or a letter of TSO Design Approval does not necessarily convey approval for installation. [2] Similar standards are maintained by other aviation authorities. For example European Technical Standard Orders (ETSO) by EASA for the European Union, [3] with limited reciprocal equivalence on a per-country ...
typos – for example: the article is Pharaoh, but you can get there from Pharoah, Pharoh, and ; singular vs. plural – Pharaohs will also go to the article; in the other direction, someone typing bagpipe or Anglo-saxon will be taken to the article with an -s on the end. inflected forms – forms like pharaonic also go to the article
The second sentence of this article contradicts AS9102. The second sentence refers to the "testing of a pre-production sample", but AS9102 section 5.1 specifically states: "5.1 First Article Inspection (FAI) shall be performed for a new part representative of the first production run.
The manufacture of biologics is considered to differ fundamentally from that of less complex chemicals, requiring a somewhat different approval process. Generic drugs that have already been approved via an NDA submitted by another maker are approved via an Abbreviated New Drug Application (ANDA), which does not require all of the clinical ...