Posts Tagged ‘CDMS’

[Webinar] An Intro To Clinical Study Migrations

Migrating clinical studies from one database to another (such as Oracle Clinical to Oracle Clinical or Oracle Clinical to Oracle InForm or Medidata Rave), is a complex process that requires a thorough understanding of clinical data management, technology, and the regulations that govern clinical trials. Join me and my colleague, Richard Gavan, for an informational webinar […]

If You Use Siebel CTMS, Medidata Rave, Or Veeva Vault…

Then we’ve got a special webinar, just for you. On July 21, we will be having a fireside chat with our client, Alliance Foundation Trials (AFT), a research organization that develops and conducts cancer clinical trials. The chat will include a few presentation slides, so that you’re not looking at a blank screen, but much […]

Does 21 CFR Part 11 Apply To CTMS, CDMS, Or EMR/EHR Systems?

  On Thursday, April 23, 2015, we delivered a webinar on 21 CFR Part 11, based on a recent blog series. During the Q&A session at the end, someone asked the following question: Does 21 CFR 11 apply to a CTMS (clinical trial management system), CDMS (clinical data management system), EMR (electronic medical record), or […]

Oracle Clinical/RDC/TMS 5.1 Released

Oracle recently announced a new version of Oracle Clinical, Remote Data Capture (RDC), and Thesaurus Management System (TMS). Some of the enhancements in version 5.1 include: Support for Partial Source Data Verification (SDV): Oracle Clinical and RDC Onsite now support creating a risk-based SDV plan that identifies only a subset of data requiring verification in […]

Navigating The Road To Creating Custom Roles in OC/RDC

On November 13, 2014, I’ll be delivering Taking Ownership of Custom Database Roles in Oracle Clinical and RDC, a one-hour webinar that’ll cover the following topics: Reasons to create custom roles Process of creating a custom role Granting the necessary access and privileges to a new role Granting the new role to the appropriate user […]

Oops! I Just Deleted Production Data For An EDC Study

Imagine accidently deleting lots of production clinical data. What do you do? How do you recover? Those are the tough questions our client was recently faced with when one of their Oracle Clinical (OC) power users ran the Delete Study Information function in the system with the intention of deleting patient data for only a handful […]

Managing a CDMS is Hard Enough, Let Alone Complex Data Migrations

Senior Management is always looking for answers about what works, what doesn’t, and how best to design and manage clinical trials. In order to get those answers, all of your trial data needs to be in one place and in a consistent format – this is the only way to extract accurate information. But, how […]

SharePoint as a Platform in a Highly Regulated, Clinical Research Environment

Last week, Perficient presented a webinar on using SharePoint as a platform in a highly regulated environment. Tony Egl, consulting services director and Jason Bell, consulting services senior technical director—both at Perficient—presented a case study that leverages SharePoint 2010 to bring clinical processes out of a paper environment and into an electronic, auditable environment. This provided the client the ability […]