Fraud and Misconduct - the Dark Side of Science
Good Laboratory Practice (GLP) - Guidelines for the Acquisition and Processing of Electronic Raw Data in a GLP Environment °
Quality Assurance Implications for Computerized Systems following the Able Laboratories FDA Inspection
Experience with the Implementation of the EU Clinical Trials Directive - First Results of a Survey Initiated by the BVMA e.V.
Technology-Driven Forms of Quality Improvement and Technical Evolution
Development of a Professional Quality Assurance Society - The SQA Model
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