Combining Patient Records, Genomic Data and Other Data to Enable Translational Medicine

The average academic research organization (ARO) and hospital has many systems that house patient-related information, such as patient records and genomic data. Combining data from a variety of sources in an ongoing manner can enable complex and meaningful querying, reporting and analysis for the purposes of improving patient safety and care, boosting operational efficiency, and supporting personalized medicine initiatives.

Please join Perficient’s Mike Grossman, a director of clinical data warehousing and analytics, and Martin Sizemore, a healthcare strategist, for a complimentary one-hour webinar in which they will discuss:

• How AROs and hospitals can benefit from a systematic approach to combining data from diverse systems and utilizing a suite of data extraction, reporting, and analytical tools, in order to support a wide variety of needs and requests
• Examples of proposed solutions to real-life challenges AROs and hospitals often encounter

Register: http://www2.perficient.com/lifesciences/CombiningPatientRecords

Oracle AERS vs. Argus Safety

Not too long ago, Oracle AERS was the most widely-used adverse event report system. However, with the acquisition of Relsys and its safety and pharmacovigilance system in 2009, Argus Safety quickly became the go-to software for most life sciences companies. Its capabilities and comprehensiveness are unmatched.

Companies currently using Oracle AERS have expressed interest in moving to Argus Safety, but want to know more before making the jump. This webinar is meant to do just that – answer your common questions.

Please join Perficient’s Dr. Rodney Lemery, director of safety and pharmacovigilance, for a free one-hour webinar in which he will:

• Compare Argus Safety to AERS
• Cover the options of effectively migrating to Argus Safety

Register: https://cc.readytalk.com/cc/s/registrations/new?cid=797ko39igeyx

Empirica Trace vs. Argus Safety

Oracle added Empirica Trace to its product portfolio when it acquired Phase Forward in 2010. Although the safety database has successfully helped organizations meet their requirements over the years, it lacks many user-friendly features and the deep functionality that is essential in today’s highly-regulated environment. Whether the capabilities relate to system management, coding, E2B, languages, or reporting, there are many differentiators in Argus Safety that current Empirca Trace users will be able to appreciate.

Please join Perficient’s Dr. Rodney Lemery, director of safety and pharmacovigilance, for a free one-hour webinar in which he will:

• Compare Argus Safety to Empirica Trace
• Cover the options of effectively migrating to Argus Safety

Register: https://cc.readytalk.com/cc/s/registrations/new?cid=73vghet75yx8

Tips and Techniques for Improving the Performance of Validation Procedures in Oracle Clinical

Ensuring the validity of patient data in your clinical data management and EDC system is essential. However, without a way to programmatically identify discrepancies and inconsistencies, such a task can inadvertently leave bad data in your system. Through validation procedures, an endless assortment of expressions and formulas, Oracle Clinical offers the powerful ability to clean and compare patient data.

Please join Perficient’s Dr. Steve Rifkin, a leading expert in Oracle Clinical, for a complimentary one-hour webinar in which he will discuss the structure of validation procedures, as well as provide various tips and techniques for developing procedures that improve the performance of edit checks.

Register: https://cc.readytalk.com/cc/s/registrations/new?cid=q3yc3ucp4iy0

10 Things to Consider When Building a CTMS Business Case

Sponsors and research organizations are often tasked with building a business case for a clinical trial management system (CTMS) before they even evaluate the various solutions in the marketplace.  

After multiple successful Oracle Siebel CTMS implementations, Perficient has identified 10 ways you can benefit from a CTMS solution. Please join Perficient’s Param Singh, director of clinical trial management solutions, for a complimentary webinar where he will share information that you can leverage as you develop a business case for a CTMS.  

He will also demonstrate the two most popular CTMS benefits and corresponding features.

Register: https://cc.readytalk.com/cc/s/registrations/new?cid=qhp1oxc6he4g 

Automatically Retrieving and Loading Data into Siebel CTMS from Multiple CRO Partners

With more and more sponsors moving towards a clinical outsourcing model, the need to obtain data from multiple CRO partners in a standard format and place it into a sponsor’s CTMS has increased. Automatically retrieving and loading data in XML format via a custom utility and integration could be a viable solution and enable sponsors to have an accurate snapshot of all their studies at any given time.

 

Please join Perficient’s clinical trial management and application development experts for a complimentary webinar that will feature a customer case study discussing:

 

• The customer’s situation and objectives
• Business reasons for using a custom utility and integration
• Technical details and considerations
• Lessons learned

Register: https://cc.readytalk.com/r/26961dk0mena&eom

Migrating Clinical Data in Various Formats to a Clinical Data Management System

A biopharmaceutical company was seeking to migrate legacy clinical studies to Oracle Clinical, the company’s clinical data management system, in order to perform cross-study statistical analysis and comply with potential audit requests. The company’s CRO partners delivered the clinical data in a variety of file formats, including PDF, Excel, Word and SAS data sets.

Please join Perficient’s life sciences clinical data management and application development experts for a complimentary webinar that will feature a customer case study discussing:

• The customer’s situation and objectives
• Data extraction, migration and standardization process
• Quality assurance review
• Custom tools used
• Lessons learned

Register: https://cc.readytalk.com/r/fj5scniuawsi&eom

The ABCs of Clinical Trial Management Systems

Gone are the days of using spreadsheets to manage clinical trials. Fortunately, a clinical trial management system (CTMS) such as Oracle Siebel CTMS, offers an effective method for streamlining business processes, reducing cost and saving time.

 

Whether you are a sponsor running global trials or a research organization conducting hundreds of studies, we invite you to join Perficient’s Param Singh, Director of Clinical Trial Management Solutions, for a complimentary webinar that will cover:

 

• What is a CTMS and who needs one
• Key functions of a CTMS
• CTMS selection process
• System types and implementation options
• Best practices

Register: https://cc.readytalk.com/r/zmpfrf4j73r&eom 

Optimizing Siebel CTMS with Electronic Trip Reports

Completing clinical and site visit trip reports electronically through a clinical trial management system (CTMS) saves sponsors and research organizations time and money. However, due to their unfamiliarity with how they work and how 21 CFR Part 11 pertains to electronic signatures, companies shy away from utilizing electronic trip report solutions to their full capacity.

Please join Perficient’s Param Singh, Director of Clinical Trial Management Solutions, for a complimentary webinar that will cover:

• Components of trip reports
• Common trip report challenges
• Live demo of trip report completion and approval process in Siebel CTMS

Register: https://cc.readytalk.com/r/drs6kmqa77tf&eom

Oracle Siebel CTMS Open UI Overview

Learn about Siebel Clinical Open UI, the latest release of Oracle’s clinical trial management system (CTMS).