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Library Management in Oracle InForm

Prior to the inception of Copy Groups, copying objects from a library or study to another study in Oracle Clinical was a slow, tedious process in which all objects had to be copied individually. Copy Groups can contain forms, form layouts, derivation and validation procedures, completion guidelines, and help text. Copy Groups allow objects to […]

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Generating SDTM Datasets in Oracle InForm

Those conducting clinical trials using EDC systems such as Oracle Clinical Remote Data Capture and Oracle InForm, face the challenge of converting their eCRF data into CDISC’s SDTM domain datasets. Regardless of the system you are using, most companies have adopted standard data collection objects. Companies are adapting to follow the CDASH guidelines, to reduce […]

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Clinical Study Migrations: Technical Things to Consider

There are a number of essential technical considerations that should be evaluated when migrating clinical studies from one database to another. Is the target database new or does the incoming data need to be “merged” into an existing database? What if the source application has been customized? What obstacles can be expected? Where does regulatory […]

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[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 […]

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Top 5 Life Sciences Blog Posts From January 2017

Now that February is here, I thought it would be neat to look back at what our readers found most interesting last month. Below are the top five blog posts Perficient’s life sciences practice wrote in January – they’re ranked in order of popularity, with number one being the most viewed piece. 4 Ways You Can Improve […]

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Tomorrow: Live Oracle Data Management Workbench (DMW) Demo

When it comes to clinical trials, the consequences of bad data can be severe. Research and development becomes complicated and lives can be put at risk. The need for clean clinical data is critical for comprehensive reporting and analysis, ultimately enabling safer drugs and devices to be brought to market faster. Join us this Thursday […]

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Can We Integrate Clinical And Safety Systems In The Cloud?

  In our last “cloud fact or fiction” post, we discussed the ability to migrate clinical and pharmacovigilance data to the cloud. Let’s jump right in and talk about system integrations in the cloud. Claim #7: Clinical trial software in the cloud cannot be integrated with other systems. 

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Eat It Up! No More Self-Reporting For Clinical Trial Subjects

  Let’s face it, relying on clinical trial participants to self-report their medication intake isn’t ideal. Lots of things can go wrong. Patients can administer medication improperly, avoid taking the medication altogether, or even claim they’ve taken the medication when, in actuality, they haven’t. While there are other means of checking whether patients are taking […]

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