EDC/Data Management Services & Products
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Quality Assurance Service: Investigation Trials & Postmarketed Projects Phase I-IV
6/10/2014
The function of Chiltern's independent QA auditing group is to assess, for investigational trials or postmarketed projects (Phases I-IV), the state of compliance with ICH-GCP and/or applicable regulatory requirements, Standard Operating Procedures (SOPs), the study protocol and/or project plans.
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Clinical Development Document Management
4/23/2013
Trial Interactive is the all inclusive source for all of your clinical data management needs. In addition to hosting clinical trial solutions and electronic case site solutions, we also provide a full array of scanning and clinical document management services.
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Safety Technology
12/21/2012
From smart, technology-driven products like our hosted Oracle Argus safety database, Oracle Interchange, Oracle Argus Insight, the Transperfect Trial Interactive safety portal, the UL Eduneering Training platform, EDC integrations, electronic data migrations, EasyCode™ Dictionary Management Tool and more to expert-infused services that deliver validation, CFR 21 Part 11 compliance, a technology support desk, system upgrades, and resolution to functional gaps to improve safety work flows, Sentrx’s Technology Services Group always delivers two essential outcomes: confidence and trust.
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Clinical Product Safety
12/21/2012
Given the complex nature of medicines and the associated unpredictability of adverse events, pharmacovigilance activities play a critical role in managing the risks posed to the general population.
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Adverse Event Management
12/21/2012
At Sentrx, we run the gamut, covering every aspect of pharmacovigilance for all stages of development and all sizes of clients. Whether your circumstances are more heavily influenced by clinical needs or post-marketing surveillance requirements or you are examining drug safety as part of your New Drug Application planning or preparing to implement risk mitigation strategies, Sentrx has the expertise to make your drug safety operations more flexible, cost-effective, and efficient.
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Panther-EDC™
11/9/2011
Panther-EDC™ integrates end-to-end study management with electronic data capture, resulting in a unified clinical data management platform that brings efficiency, quality, and versatility to trials of all types.
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Integrated Clinical Trial/Electronic Health Record Data Platform - Prism®
11/8/2011
While the United States lags behind international adoption rates for electronic health records, the federal government’s financial reward for “meaningful use” of technology is quickly changing that scenario.
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ClinPlus Data Management
10/3/2011
For more than 15 years, ClinPlus® Data Management software (CPDM) and services have helped clients in the pharmaceutical, biotechnology, medical device and contract research industries manage clinical studies across multiple therapeutic areas and collect quality data, while meeting strict timelines and staying within budget.
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Clinical Data Management
6/24/2011
At Theorem Clinical Research, our team of global Clinical Data Management (CDM) experts are committed to upholding a standardized, process-driven approach. As a customer-focused operation, we feature a robust service portfolio and strive to ensure the highest quality results on every project.
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Data Management Services
6/22/2011
SGS’s Data Management team has over 15 years of experience providing unparalleled service with an understanding for individual clients’ needs.