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Who and Why?
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| CONFERENCE WHY ATTEND? REGISTRATION
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Who should attend? This
programme is intended for pharmaceutical and contract research professionals who are
interested in facilitating, managing and transferring clinical trial data. Those
interested in capturing more accurate and timely clinical trials data are urged to attend,
including Directors, Heads and Managers of Data Management, Clinical Trials, Biometrics,
Information Technology and Contract Research. Why go to an IIR event? This conference programme has been extensively researched with your peers. This means that the event is tailored exactly to meet the key issues and challenges you asked to see addressed, with presentations from people you want to hear. There will be major contributions from all the following pharmaceutical and Clinical Research Organisations: • MERCK SHARPE & DOHME • EUROPEAN COMMISSION • PPD PHARMACO • HOECHST MARION ROUSSEL • MERZ & CO GMBH • SANKYO PHARMACEUTICALS • SOLVAY PHARMACEUTICALS • ZENECA PHARMACEUTICALS • MDS HARRIS • GLAXO WELLCOME • PFIZER CENTRAL RESEARCH • LABORATOIRES PIERRE FABRE • CLINTRIALS RESEARCH • BASF PHARMA •KNOLL PHARMACEUTICALS • BRISTOL-MYERS SQUIBB • REMOTE DATA ENTRY LTD • COMPUTER SCIENCE CORPORATION SCHERING AG • ROCHE BIOSCIENCES USA • BAYER PLC • QUINTILES • COVANCE CAPS • IBAH • COOPERS & LYBRAND • VERUM TIL OCCUM • We believe that this conference offers you the best value in time and money spent, giving you the practical information and insights you seek from key organisations, on the crucial issues you face in clinical data management. For further information on the programme, please contact Zoe Bowers, Conference Director, on +44 (0)171 915 5074/email:zoeb@iirltd.co.uk
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