Good practice in the postmarketing surveillance of medicines
- PMID: 9297731
- DOI: 10.1023/a:1008610722972
Good practice in the postmarketing surveillance of medicines
Abstract
In addition to Good Clinical Trial Practice for the study of experimental drugs, regulations are also needed for good practice in the assessment of medicines after approval (Good PMS Practice, GPP). GPP has to protect the interests of public health at large as well as those of individual patients, investigators and pharmaceutical companies. GPP may be the natural way to solve threatening conflicts between privacy legislation and the public interest.
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