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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]
CRL for a revoked cert of Verisign CA. There are two different states of revocation defined in RFC 5280: Revoked A certificate is irreversibly revoked if, for example, it is discovered that the certificate authority (CA) had improperly issued a certificate, or if a private-key is thought to have been compromised.
Since an OCSP response contains less data than a typical certificate revocation list (CRL), it puts less burden on network and client resources. [10] Since an OCSP response has less data to parse, the client-side libraries that handle it can be less complex than those that handle CRLs. [11]
Ensuring continuous, long-term access to "last-copy" paper and microform collections for the CRL community through coordinated archiving and collection-sharing arrangements with key partners. [ 2 ] In 2008, the Center for Research Libraries was awarded a $1.45 million grant from the Andrew W. Mellon Foundation to support this initiative.
Certificate revocation list, in computing, a list of revoked certificates; Chemistry Research Laboratory, University of Oxford, the main chemistry building at Oxford University; Complete Response Letter, the official FDA response to a New Drug Application; Crown-rump length, the ultrasound measurement of a foetus
It was the largest qui tam (whistleblower) settlement paid by a medical lab for manufacturing and distributing a faulty product. [51] In May 2011, Quest paid $241 million to the state of California to settle a False Claims Act case that alleged the company had overcharged Medi-Cal , the state's Medicaid program, and provided illegal kickbacks ...
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A certificate of analysis (COA) is a formal laboratory-prepared document that details the results of (and sometimes the specifications and analytical methods for) one or more laboratory analyses, signed—manually or electronically—by an authorized representative of the entity conducting the analyses. This document gives assurances to the ...