Posts Tagged ‘Oracle InForm’

Over the last few years, Oracle has been hard at work developing its newest flagship clinical trials platform called Clinical One. The company has invested a significant amount of money and personnel in building the platform. While there are many more capabilities to come over the next few years, you can already leverage Clinical One […]

I recently shared a project in which we helped a pharmaceutical company build studies in Oracle InForm. Today, I want to share a project that has to do with the length of time it took for a major pharmaceutical company to run Oracle InForm reports, which caused significant problems, including delays in being able to […]

The beauty of having a versatile team of clinical data management experts is that they understand the life sciences industry and how companies operate. Through client projects and having worked at pharma companies in previous roles, they know the many unique challenges and needs of pharmaceutical and medical device companies. Equally important, they’re also technologists. […]

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 […]

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 […]

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 […]

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 […]

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 […]

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 […]

  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. 

  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 […]