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ClinDatrix, Inc

The Experience of Big. The Advantage of Value.

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      • Louise M. Murphy, PhD, MBA, CQA
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  • 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

Infectious Disease

Home » Infectious Disease

ClinDatrix: Expertise in Infectious Diseases Clinical Trials

With over two decades of experience in clinical trial management, ClinDatrix is a trusted partner for clinical research across all phases (I–III). Our staff has experience in infectious diseases, including herpes zoster, dysentery, flu vaccines, gram-positive infection (pediatric), sepsis, traveler’s diarrhea, and vancomycin-resistant infection.

Leveraging deep expertise in protocol development, electronic data capture (EDC) systems, and clinical trial logistics, our team ensures methodical execution of infectious disease trials. 

Key Highlights of ClinDatrix Infectious Disease Research Expertise

  • Agility in Study Management: We design and deploy study databases on our secure servers within 5 weeks—well ahead of the industry standard of 12 weeks—and implement protocol adjustments within 1–2 days, allowing us to adapt quickly to evolving study needs.
  • Regulatory and Compliance Excellence: Our team ensures full compliance with rigorous regulatory and ethical standards, providing sponsors with the assurance of high-quality trial execution.
  • Operational Precision: From eCRF design to final data analysis, our comprehensive support equips sponsors to confidently and efficiently achieve their research objectives.

Partner with ClinDatrix today to advance your infectious disease research. Backed by a proven track record and a commitment to operational excellence, we deliver tailored solutions to the unique challenges of infectious disease clinical trials. Contact us today to learn more!

Service Codes

  • BI = Biostatistics
  • CL = Clinical
  • DM = Data Management
  • FS = Full Service
  • MS = Medical Safety
  • MW = Medical Writing
  • RA = Regulatory Affairs
PhaseIndicationServicesSitesPatients
1HerpesDM5700
1ZosterFS18

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

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