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Function overview: Adjusts templates based on provided JSON configuration files. This request is limited to Template:Cite news and Template:Cite web, and is primarily intended to correct issues where the work or publisher is linked to the wrong target. Automatic, Supervised, or Manual: Automatic Programming language(s): Python
If the reply is in the affirmative, I send the following message. Note that I repeat the file name in case they forget it from my first message. The content under the final heading " File name on Wikimedia Commons" is to increase the chance that a downloader will attribute the copyright holder – it's a personal preference only. Hello [firstname],
Download as PDF; Printable version; In other projects ... This template is for use by editors who are requesting permission; ...
In general, if you want to make an edit request: Propose a specific change on a talk page.Don't add an edit request template yet.; Once there is consensus for the change, and any final details have been worked out, put a template on the talk page along with a short, clear explanation.
In public key infrastructure (PKI) systems, a certificate signing request (CSR or certification request) is a message sent from an applicant to a certificate authority of the public key infrastructure (PKI) in order to apply for a digital identity certificate. The CSR usually contains the public key for which the certificate should be issued ...
In a manufacturing environment, a request for waiver (RFW) is a request for authorization to accept an item which, during manufacture or after inspection, is found to depart from specified requirements, but nevertheless is considered suitable for use as is or after repair by an approved method.
Fast track is a designation by the United States Food and Drug Administration (FDA) of an investigational drug for expedited review to facilitate development of drugs that treat a serious or life-threatening condition and fill an unmet medical need.
In United States pharmaceutical regulatory practice, a Complete Response Letter (CRL), or more rarely, a 314.110 letter, is a regulatory action by the Food and Drug Administration in response to a New Drug Application, Amended New Drug Application or Biologics License Application, indicating that the application will not be approved in its present form. [1]