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An electronic signature, or e-signature, is data that is logically associated with other data and which is used by the signatory to sign the associated data. [1] [2] [3] This type of signature has the same legal standing as a handwritten signature as long as it adheres to the requirements of the specific regulation under which it was created (e.g., eIDAS in the European Union, NIST-DSS in the ...
Example of a corporate seal. In this case, the word "seal" is also used as visual pun: an image of the marine animal of the same name appears on the device. A company seal (sometimes referred to as the corporate seal or common seal) is an official seal used by a company.
For an electronic signature to be considered as advanced it must meet several requirements: [3] [4] The signatory can be uniquely identified and linked to the signature; The signatory must have sole control of the signature creation data (typically a private key) that was used to create the electronic signature
A digital signature is a mathematical scheme for verifying the authenticity of digital messages or documents. A valid digital signature on a message gives a recipient ...
A qualified electronic signature is an advanced electronic signature with a qualified digital certificate that has been created by a qualified signature creation device (QSCD). For an electronic signature to be considered as a qualified electronic signature, it must meet three main requirements: First, the signatory must be linked and uniquely ...
(8) Electronic signature - means an electronic sound, symbol, or process attached to or logically associated with a record and executed or adopted by a person with the intent to sign the record. Another important aspect of this definition lies in the necessity that the electronic signature be linked or logically associated with the record.
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This guidance supersedes the guidance of the same name dated April 1999; and supplements the guidance for industry on Part 11, Electronic Records; Electronic Signatures — Scope and Application and the Agency's international harmonization efforts when applying these guidances to source data generated at clinical study sites.
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