How can the quality of medical data in pharmacovigilance, pharmacoepidemiology and clinical studies be guaranteed?

Alla, François; Rosilio, Myriam; Funck-Brentano, Christian; Barthélémy, Philippe; Brisset, Sophie; Cellier, Dominic; Chassany, Olivier; Demarez, Jean-Paul; Diebolt, Vincent; Francillon, Alain; Gambotti, Laetitia; Hannachi, Hakima; Lechat, Philippe; Lemaire, François; Lièvre, Michel; Misse, Christophe; Nguon, Marina; Pariente, Antoine; Rosenheim, Michel; Weisslinger-Darmon, Nadine

Alla, François; Rosilio, Myriam; Funck-Brentano, Christian; Barthélémy, Philippe; Brisset, Sophie; Cellier, Dominic; Chassany, Olivier; Demarez, Jean-Paul; Diebolt, Vincent; Francillon, Alain; Gambotti, Laetitia; Hannachi, Hakima; Lechat, Philippe; Lemaire, François; Lièvre, Michel; Misse, Christophe; Nguon, Marina; Pariente, Antoine; Rosenheim, Michel; Weisslinger-Darmon, Nadine.

Affiliation

Alla F; Université de Lorraine, Nancy, France.

Therapie ; 68(4): 209-23, 2013.

Article in En, Fr | MEDLINE | ID: mdl-23981258

Subject(s)

Clinical Trials as Topic; Databases, Factual/standards; Pharmacoepidemiology; Pharmacovigilance; Quality Assurance, Health Care/methods; Adverse Drug Reaction Reporting Systems/standards; Data Collection; Humans; Practice Guidelines as Topic; Quality Assurance, Health Care/statistics & numerical data; Research Design/standards

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Full text: 1 Database: MEDLINE Main subject: Quality Assurance, Health Care / Clinical Trials as Topic / Databases, Factual / Pharmacoepidemiology / Pharmacovigilance Type of study: Guideline Limits: Humans Language: En / Fr Journal: Therapie Year: 2013 Type: Article Affiliation country: France

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