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General Principles for NICHD Clinical Research

The NICHD strives to abide by the following general principles in its design and conduct of clinical research.

Transparency

The NICHD will ensure transparency by:

  • Openly sharing what, how, where, and when we engage in clinical research projects
  • Committing to timely public dissemination of research results in an appropriate and understandable manner

Quality

The NICHD will ensure quality in:

  • The types of interactions between NICHD and stakeholders
  • The scientific advice offered
  • Clinical research review
  • Study design
  • Clinical research process
  • Presentation and reporting of results

Integrity

The NICHD will ensure integrity in:

  • Review of study proposals
  • Implementation of study protocols
  • Conduct of clinical research
  • Collection, preservation and analysis of data
  • Evaluation of study results
  • Formulating recommendations

Trust

The NICHD will ensure trust:

  • From study participants in the planning, oversight and conduct of clinical research to respect and protect their interests
  • Among investigators and study personnel through commitment to shared goals and quality of study implementation
  • Between investigators and the NICHD through the fair allocation of resources based on consensus public health priorities and scientific opportunities, willingness to listen and support, and providing unbiased scientific advice
  • Among NICHD staff through shared goals and transparency about the basis for decision making
  • Between the NICHD and stakeholders by acting as responsible trustees of public resources and research agenda

Transparency, Quality, Integrity and Trust are our T(i)QIT (“TICKET”).

Last Updated Date: 03/06/2007
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