8 Matching Annotations
  1. Nov 2016
    1. We propose that all publicly available clinical research data objects should have a DOI assigned, so that they have a unique identifier.

      I like that idea: Give study documents and study datasets DOIs in the same ways other data objects such as this journal article http://dx.doi.org/10.1186/s13063-016-1686-5

      Can this be done already in internal document mgmt systems. DocID in Documentum for the main document of a CSP, CSR, Informed Consent get a DOI??

    2. In practical terms, almost all studies will have multiple identifiers associated with them – some public, such as registry IDs and the identifiers assigned by regulatory authorities, and others internal, such as the IDs used by sponsors and funders.

      Need ways to publish verified statements on different identifiers referring to the same study see also my blog post http://kerfors.blogspot.se/2016/11/opentrials.html

    3. Registry identifiers (IDs): Most (but not all) clinical trials are entered prospectively into publicly accessible trial registries such as ClinicalTrials.gov. That provides them with a PID that is unique when coupled with an identifier for the registry (normally its URL or an abbreviation).

      A study registry ID as a text string, e.g."NCT01732822" and as a URL, e.g. https://clinicaltrials.gov/ct2/show/NCT01732822 see my blog post http://kerfors.blogspot.se/2016/11/opentrials.html asking for clarifications of the differences between study Page URLs and Study URIs in OpenTrials

  2. Aug 2016
  3. Jun 2016
  4. Mar 2015