CROS NT

A Data-Driven CRO

  • About Us
    • Who We Are
    • Testimonials
    • Management
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    • Quality Assurance
  • Outsourcing Solutions
    • Centralized Biometrics
    • Functional Service Provider
    • Full Service
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  • BIOMETRICS
    • Clinical Data Management
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    • Statistical Programming
    • Medical Writing
    • Pharmacovigilance
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  • eCLINICAL
    • EDC Portfolio
    • eCOA
    • CTMS
    • IWRS
  • DATA-DRIVEN SOLUTIONS
    • CROScheck™
    • Data Anonymization
    • Risk-Based Monitoring
  • REGULATORY & CLINICAL
    • Regulatory Affairs
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    • Clinical Monitoring
  • EXPERTISE
    • Phase I-IV Studies
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    • Integrated Summaries
    • CDISC

CRO

How to keep Integrated Summaries (ISS/ISE) projects under control

    • Blog
    • date: 05 February 2018
    • hs_social:
  • CRO, integrated summaries, regulatory submissions

Conducting Clinical Trials in the Era of Data Privacy and Anonymization

    • Blog
    • date: 18 January 2018
    • hs_social:
  • Clinical Trial Regulation, CRO, data anonymization, GDPR, transparency

Clinical Trial Outsourcing strategy and trends in 2018: Focus on technology, data transparency and oversight

    • Blog
    • date: 10 January 2018
    • hs_social:
  • clinical outsourcing, CRO, data anonymization, GDPR

[INFOGRAPHIC] – CROS NT Celebrates 25 Years in Business as a data-driven CRO

    • Blog
    • date: 29 December 2017
    • hs_social:
  • 25 years in business, biometrics, CRO

Tools and Processes for Data-Driven Monitoring and a Risk-Based Approach

    • Blog
    • date: 08 May 2017
    • hs_social:
  • clinical trials, CRO, ICH GCP E6 (R2), Risk-Based Approach, Risk-Based Monitoring

[INFOGRAPHIC] ICH GCP E6 (R2) Addendum: Risk-Based Approach and What to Know

    • Blog
    • date: 30 April 2017
    • hs_social:
  • CRO, ICH GCP E6 (R2), Risk-Based Approach, Risk-Based Monitoring

[INFOGRAPHIC] Negotiating a Successful FSP Contract with your Provider

    • Blog
    • date: 28 April 2017
    • hs_social:
  • clinical trials, CRO, FSP, Functional Service Provision

How Biometrics can support a Risk Based Monitoring Approach for ICH GCP E6 (R2) Guidelines

    • Blog
    • date: 20 April 2017
    • hs_social:
  • CRO, Good Clinical Practice, ICH GCP E6 (R2), Risk-Based Monitoring

Blog

    • date: 17 April 2018
    • hs_social:
  • adaptive trial design, biostatistics, oncology research

[INFOGRAPHIC] Making Effective Use of Adaptive Designs in Early Oncology Trials

    • date: 06 April 2018
    • hs_social:

Working with your CRO to Conduct Efficient Respiratory Trials

    • date: 29 March 2018
    • hs_social:
  • data anonymization, de-identification, EDC, GDPR

[INFOGRAPHIC] EDC System Data Privacy Compliance Considerations

Legal

Copyright CROS NT
Contract Research Organization.
All Rights Reserved.
Imprint/Legal Disclaimer

Contact

Beechwood
Grove Park
White Waltham
Maidenhead
SL6 3LW
Tel: +44 (0) 1628 290141
Mail: info@crosnt.com

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