Challenges and progress in adverse event ascertainment and reporting in clinical trials
Lassere, M. N. D., Johnson, Kent R., Woodworth, T. G., Furst, D. E., Fries, J. F., Kirwan, J. R., Tugwell, P. S., Day, R. O., Brooks, P. M.
Giving and receiving of gifts between pharmaceutical companies and medical specialists in Australia
McNeill, P. M., Kerridge, I. H., Henry, D. A., Stokes, B., Hill, S. R., Newby, D., MacDonald, G. J., Day, R. O., Maguire, J. M., Henderson, K. M.
Medical specialists and pharmaceutical industry-sponsored research: a survey of the Australian experience
Henry, David Alexander, Kerridge, I. H., Hill, Suzanne, McNeill, P. M., Doran, Evan, Newby, David A., Henderson, Kim M., Maguire, Jane, Stokes, Barrie J., Macdonald, G. J., Day, R. O.
Standardized assessment of adverse events in rheumatology clinical trials: Summary of the OMERACT 7 Drug Safety Module update
Lassere, M. N. D., Johnson, Kent R., Boers, M., Carlton, K., Day, R. O., de Wit, M., Edwards, I. R., Fries, J. F., Furst, D. E., Kirwan, J. R., Tugwell, P. S., Woodworth, T. G., Brooks, P. M.
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