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ClinDatrix, Inc

The Experience of Big. The Advantage of Value.

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      • Louise M. Murphy, PhD, MBA, CQA
      • Brian G. Murphy, BEng, PhD
      • Steve O. Balyakin, MD, PhD, FFPM, CMC
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    • Harnessing the Power of Oracle InForm with ClinDatrix
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  • Contact Us
  • About Us
    • Leadership
      • Louise M. Murphy, PhD, MBA, CQA
      • Brian G. Murphy, BEng, PhD
      • Steve O. Balyakin, MD, PhD, FFPM, CMC
    • Quality
    • Infrastructure
    • Strengths
    • News & Events
    • Privacy Policy
  • Services
    • Clinical Trial Project Management
    • Clinical Trial Investigator Meetings & Event Planning
    • Clinical Trial Monitoring
    • Clinical Trial Medical Monitor & Medical Safety
    • Clinical Trial Data Management
    • Clinical Trial Biostatistics
    • Medical Writing Services
    • Clinical Regulatory Affairs
    • Quality Assurance for Clinical Trials
    • Clinical Trials Consultant
      • Engineering
      • Data Management
      • Biostatistics Consulting
  • Therapeutic Areas
  • Medical Devices
  • Technology
    • Harnessing the Power of Oracle InForm with ClinDatrix
    • SAS
    • NQuery
    • IRT, IWRS
  • Global Affiliates
    • Venn Life Sciences
    • DOT International
    • OnQ Research
    • Research & Development RA S.A.
    • IPSUM
    • Q-Trials
    • ClinGroup
    • Q2 Business Intelligence
    • ComboTrial
  • Contact Us

Technology

Home » Technology

To ensure the safety and integrity of our clients’ data, ClinDatrix has invested heavily in proven and proprietary systems for clinical research. We also employ a staff of IT specialists to sustain the validation, reliability and functionality of our systems.

We dedicate significant resources to our technology because it is the foundation of our business. The systems listed in the left navigation pane have the power and flexibility to handle small to large amounts of data as well as simple to complex study designs. All systems are hosted in a secure environment. Click the data sheet in the left pane for a list of key features.

Quality Assurance

The equipment and systems selected by ClinDatrix are implemented in accordance with good scientific and technological practices. Our fully validated (IQ/OQ/PQ) clinical research systems provide a secure, parallel processing environment that meets all regulatory agency requirements. All validation documentation is available for client review by appointment at ClinDatrix headquarters.

Change Control

All the computer systems that manipulate clinical data are called “GxP” systems and are under Change Control. Change Control procedures rigorously follow an SOP with forms required to be approved in writing before even minor changes, such as disk or memory changes, can be made. Even Windows security updates to GxP servers at ClinDatrix are under Change Control.

System Safeguards

ClinDatrix maintains fully secured facilities within a professional class office building in the Irvine Spectrum in Irvine, CA. The two-story building is securely locked after business hours and patrolled at night and on weekends by a security company. We assure the safety and security of our offices, file room and servers via SOPs and strict company practices. Our working environment complies with Good Clinical Practice and is a validated systems environment per FDA regulations and guidance. Our GxP systems are governed by documented change control.

Our network infrastructure management includes defined SOPs, software change control and system validation support. We also have a disaster recovery site at a data center 240 miles from our facility, and we sustain an active disaster recovery planning and testing program.

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ClinDatrix, Inc. * 19 Rosana Way * Coto de Caza, CA 92679 * Tel: 949.235.4045

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