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Right Around The Corner: Oracle Health Sciences Connect 2019

Oracle Health Sciences Connect is a unique conference that brings thought leaders together to share deep industry knowledge and best practices that revolve around clinical and safety applications. This year, the event takes place in Philadelphia from April 9–10, 2019. Perficient will deliver three presentations throughout the conference, and we invite all of you to […]

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Join Us At Oracle Industry Connect 2018

Perficient is sponsoring Oracle Industry Connect April 10-11 in New York City, and we would like our valued clients to be there. Several key representatives from our life sciences practice will be available to discuss any of your ongoing or upcoming initiatives. Mike Grossman, General Manager Dennis Dougherty, Business Development Executive Rudolf Coetzee, Business Development […]

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Top 5 Pharma & Medical Device Blog Posts From December 2017

Now that January 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 December – they’re ranked in order of popularity, with number one being the most viewed piece. Shared Investigator Platform (SIP) Struggles […]

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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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Oracle Data Management Workbench Overview And Use Cases

This Thursday, Perficient is hosting a webinar on Oracle Data Management Workbench (DMW) alongside Oracle, one of our most valued partners. From Perficient, we’ll have Prabha Ranganathan, the director of clinical data warehousing and analytics, and from Oracle, we’ll have Srinivas Karri, the director of product strategy for DMW. Yesterday, I got a sneak peek […]

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Using Oracle DMW To Solve Clinical Data Review Challenges

In part one of this two-part blog series, we outlined a number of challenges that organizations face with clinical data reviews. In today’s post, part two of the series, we’ll take a look at how Oracle Health Sciences Data Management Workbench (DMW) can be used to tackle those challenges. DATA MANAGEMENT WORKBENCH (DMW) OVERVIEW When […]

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Key Challenges Our Clients Face With Clinical Data Review

When it comes to clinical trials, bad data can result in severe consequences. Research and development can become more complicated and lives can be put at risk. Clean clinical data is critical for accurate analysis and reporting, ultimately enabling safer drugs and devices to be brought to market faster. In this two-part blog series, we’ll […]

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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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Oh My, Where Has The Time Gone?

Next week, we are exhibiting at Oracle Industry Connect (OIC) 2017 in Orlando, Florida. For those not familiar with OIC, it is a conference dedicated to a variety of verticals, including Life Sciences and Healthcare. Prior to the existence of OIC, the Annual Oracle Health Sciences User Group (OHSUG) Meeting was an event devoted to users […]

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Importance Of User Interface Design When Reviewing Clinical Data

In the previous post, I talked about varying levels of scrutiny for data review and what happens when recording the user actions. In this post, I will talk about the importance of the user interface for a review. Successfully navigating requirements, design, development, testing, user acceptance and ongoing support of any application requires user involvement […]

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Recording Review Actions During A Clinical Data Review

As was mentioned in a previous post, providing an easy-to-use interface is important for data review, including filtering, audit data, and User Review Action buttons. The user actions buttons initiate recording that all, or a portion, of a review has been performed. In the previous section, we mentioned a Review Timestamp, which is one of […]

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Identifying Which Data To Review During A Clinical Data Review

In my last blog post, I presented some thoughts on showing data changed since last review. Today, we will concentrate on the level of scrutiny and what happens when recording the user actions in the review. Not all data may require the same level of scrutiny during a review. Additional focus may need to be […]

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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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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 […]

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What To Do When An Outsourced Clinical Trial Hits A Roadblock

  Let’s face it: Keeping clinical trials on schedule is not easy to do. Whether a sponsor runs into issues with quality, timeline, personnel, or myriad other things with an outsourced partner, it’s crucial to address the problems as soon as they’re identified. There are a few routes a sponsor can take when a study […]

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Ready To Validate Oracle Clinical/RDC/TMS 5.1? We Are!

  Last November, I wrote about the new release of Oracle Clinical, Remote Data Capture (RDC), and Thesaurus Management System (TMS), version 5.1. As many companies continue to run these “tried-and-true” clinical data management and EDC systems, the enhancements were quite welcome. Since then, our data management team has been developing a complete Validation Suite […]

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Migrating Legacy Clinical Data From CRO To Sponsor

  Sponsors are known to work with multiple contract research organizations (CROs). And, depending on the agreement in place with each CRO, data can be captured in either the sponsor’s systems (CDMS and/or EDC) or the CRO’s. If the data is stored in CRO databases, there may come a time when it needs to be […]

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Can Your Clinical And Safety Data Join You In The Cloud?

  In our last “cloud fact or fiction” post, we identified several reasons why hosting clinical and pharmacovigilance systems is just as safe as housing them on-premises. In fact, in many cases it could prove to be safer. This week we’ll briefly discuss migrating data to the cloud. 

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Perficient’s Top 5 Life Sciences Blog Posts From January 2015

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. 6 Trends In Life Sciences […]

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