Study a greater technique to put together scientific trial information for reporting and evaluation. —
Many corporations have made nice strides in standardizing and conforming topic information collected in scientific trials, in an effort to have a extra environment friendly and repeatable approach of delivering the info to reporting programs for statistical evaluation and regulatory submissions.
Sometimes, getting ready information is made up of the next three steps:
1. Specifying the conformed information
2. Programming the conformed specification
3. Validating the written packages work as anticipated
Please be a part of BioPharm Programs’ Michael Grossman, vice chairman of scientific information warehousing and analytics, for a complimentary one-hour webinar that may talk about and display one technique to dramatically cut back the trouble of specification and validation, in addition to take away the programming step in its entirety. The following packages are routinely generated in Oracle Life Sciences Knowledge Hub (LSH) and as standalone SAS. The tip result’s a big improve within the productiveness of knowledge preparation and conforming for inside use, together with runnable packages that may be despatched to regulatory authorities and companions.
To view this webinar in its entirety, please go to: or