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Updated: Aug 6, 2026
14:32
Using Visual and Narrative Methods to Achieve Fair Process in Clinical Care
Published on: February 16, 2011
[Good clinical practice:impediment of source of progress?]
1Agence nationale de recherches sur le sida, Paris.
La Revue Du Praticien
|June 30, 2000
Summary
France
Area of Science:
- Clinical trial regulation
- Medical research ethics
- Public health policy
Context:
- French and European laws, including the Huriet-Sérusclat Law (1988) and data protection regulations, govern clinical trials.
- These regulations enhance trial quality and participant safety.
- They have also improved clinical care through better patient information and protocol adherence.
Purpose:
- To analyze the impact of the legal and regulatory framework on clinical trials in France.
- To discuss the challenges and opportunities for future clinical trial organization.
Summary:
- Extensive legal and regulatory frameworks in France have improved clinical trial quality and patient safety.
- However, increased complexity and cost now limit clinician-led trials.
- There is a need for health authorities to support public health-focused therapeutic strategy trials.
Impact:
- Improved scientific rigor and participant security in clinical research.
- Enhanced physician training in patient communication and protocol adherence.
- Increased costs and complexity necessitate new models for supporting public health clinical trials.
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