Search for 'clinical data' returned 30 results
Most requested webinar topics
A while back we have launched the Request a webinar feature, so that our visitors can tell us what they are interested in. To all webinar hosts out there, here are t...
Open source technologies to run efficient clinical trials
Live demo of ClinCapture, Clinovo's open source electronic data capture (EDC) system The development of open source technology in the clinical arena has been rapi...
$145
Recent Federal Regulations Affecting Employee Benefits
Overview : This presentation will provide attendees with an introduction to some of the many new regulations relating to employee benefits, with a focus on regulatio...
The Ins and Outs of CTMS Data Migration
You are considering implementing a new clinical trial management system (CTMS), or maybe you have already made the decision. But you are wondering: What should we do...
Oracle Clinical / Remote Data Capture Implementation Standards and Best Pra...
As your organization implements or upgrades to a newer version of Oracle Clinical (OC) and Remote Data Capture (RDC), there are many considerations to take into acco...
$189
21 CFR Part 11 Add-On Inspections by the FDA
In December 2010 the FDA began a project to better understand the industry’s adherence (or lack thereof) to 21 CFR Part 11. This involves the ‘add on’ surveill...
$189
Managing high-enrolling sites: CRO’s perspective
Description Why should you Attend: In the mutli-site cinical studies, it is quite common that one or more sites in several coutnries become high enrollers. T...
Open Source Technologies for Clinical Trials
Eric Morrie, Manager for Clinical Programming at Abbott Vascular, shares his expertise in open source systems for clinical trials Open source is becoming more and...
CDISC® SDTM Conversion
The mission of CDISC is to develop and support global, platform-independent data standards to improve medical research. As a CDISC Gold Member, Clinovo has been cont...
Medidata Rave® Custom Functions
Configuring a clinical EDC study in Medidata Rave is simple with good training. Study builders can easily configure eCRFs and review complex edit checks and derivati...
The New Face of Personalized Medicine: Targeting Disease Diagnostics and Tr...
Thanks to stunning progress in technology development and biomedical research, we have more preventive, diagnostic, and treatment alternatives for human diseases tha...
$1299
Computer System Validation – Reduce Costs and Avoid 483s
This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated envi...
Open Source Technologies for Clinical Trials
Open source is becoming more and more prevalent in clinical trials, introducing an innovative way to save costs while keeping high clinical data quality and security...
$189
Excel Spreadsheet Compliance with 21 CFR 11
Excel Spreadsheet Compliance with 21CFR11 Description This course will describe the regulatory and business requirements for Excel spreadsheets, using example...
Open Source Technologies for Clinical Trials
Open source is becoming more and more prevalent in clinical trials, introducing an innovative way to save costs while keeping high clinical data quality and security...
CDISC® SDTM Conversion
The mission of CDISC is to develop and support global, platform-independent data standards to improve medical research. As a CDISC Gold Member, Clinovo has been cont...
$189
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ...
Summary This Medical Device training will be discussing the newly-updated requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Dire...
Implementing the Rave Custom Functions Best Suited to your Clinical Study R...
Configuring a clinical EDC study in Medidata Rave is simple with good training. Study builders can easily configure eCRFs and review complex edit checks and derivati...
CDISC Express Demo
Discover CDISC® Express, our free innovative SDTM mapping tool. CDISC Express is a free SAS application that automatically converts clinical data into CDISC SDTM u...
Open Source Technologies for Clinical Trials
Eric Morrie, Manager for Clinical Programming at Abbott Vascular, shares his expertise in open source systems for clinical trials Open source is becoming more and...
Flexible Study Design in Oracle Clinical and Remote Data Capture 4.6
Oracle Clinical (OC) / Remote Data Capture (RDC) 4.6 provides the ability to conduct global clinical trials more efficiently and effectively. The newest release feat...
CDISC Express Demo
Discover CDISC® Express, our free CDISC SDTM mapping tool and learn how to speed up your clinical trial process. CDISC is a global, non-profit organization that ...
Implementing the Rave Custom Functions Best Suited to your Clinical Study R...
Configuring a clinical EDC study in Medidata Rave is simple with good training. Study builders can easily configure eCRFs and review complex edit checks and derivati...
Free CDISC mapping tool for clinical trials
Clinovo developed a free open source tool to convert data into CDISC SDTM standards to speed up FDA review. This webinar will demonstrate all the features of the app...
Leveraging Oracle’s Life Sciences Data Hub (LSH) to Enable Dynamic Cr...
Oracle’s Life Sciences Data Hub (LSH) is a framework that allows sponsors and clinical research organizations to manage clinical trial research data. One of the...
Live Demonstration of Simple Forms, an Electronic Data Capture (EDC) Soluti...
Simple Forms, a low-cost and intuitive EDC system, has been implemented at biopharmaceutical, medical device, and contract research organizations since 2005. The sol...
Making Oracle Clinical and Remote Data Capture 4.6 Features Work for You
Implementation of Oracle Clinical (OC) and Remote Data Capture (RDC) 4.6 provides life sciences organizations with more options for designing clinical trials. This m...
Leveraging Oracle’s Clinical Development Analytics to Boost Productiv...
Oracle’s Clinical Development Analytics (CDA) is a comprehensive analytics solution that provides life sciences sponsors and CROs operational insight into their cl...
The Benefits of Siebel Clinical Integration
You've implemented state-of-the-art enterprise systems for different work functions, but they don't talk to each other. Now what? Savvy organizations know how to max...
$249
Establishing Global Drug Substance and Drug Product Specifications – What...
Learn how to establish global drug substance and drug product specifications that are appropriate to the phase of clinical development and market application, and un...
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