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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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