CDISC

Clinical Metadata at Phuse next week

Clinical Metadata will be presenting their metadata and projects standards tool at the PhUse conference in Edinburgh on Tuesday 10th October. Join them to learn how Clinical Metadata can help the pharmaceutical industry manage its clinical trial metadata and data…

By Andrew N | 02/10/2017 | Clinical Metadata | No Comments |

Clinical Metadata can help you manage your clinical trial metadata and achieve CDISC compliance

Clinicalmetadata.com is a new web-based tool, built of the latest technologies, designed to help you manage your clinical trial metadata, data standards and achieve CDISC compliance. The tool also generates SAS code and submission deliverables including define.xml and annotated crfs. Visit…

By Andrew N | 20/09/2017 | CDISC | No Comments |

SAS-paper-review-5/

This week our SAS paper review looks at “TIPS AND TRICKS OF EFFICIENT SAS® PROGRAMMING FOR SDTM DATA ” by Eric Qi and Fikret Karahoda of Merck & Co. The paper examines problems which can result from processing and storing large SDTM datasets and…

By Andrew N | 13/11/2014 | SAS paper review | No Comments |

CDISC- Analysis Results Metadata

CDISC have released a draft version of the Analysis Results Metadata (AResM) v1.0 for Define-XML v2 is now available for 30 day public review. Analysis Results Metadata are an extension to Define-XML v2 not part of SDTM. They illustrate which ADaM dataset…

By Andrew N | 13/09/2014 | CDISC | No Comments |

CDISC training

The first part of our CDISC training series, Introduction to CDISC, will be available to download here for free next week.

By Andrew N | 05/03/2014 | CDISC training | No Comments |

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