Rev Med Interne. 1986 Nov;11-3.
La Revue de medecine interne
[Article in French] J P Bader
PMID: 3809775
For clinical investigators, usually on the staff of university hospitals, the setting up in France of a good clinical practices system will no doubt improve the quality of clinical trials in that country. It remains that the investigator's responsibility is involved before, during and after the clinical trial period and that the demand on his time is considerable. Close co-operation between the pharmaceutical firm (as promotor and monitor) and the clinical investigator is necessary to conduct a clinical trial.