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Discussion Board: Comments & Questions

Anonymous wrote (9th Aug, 2010) Is the new ESF Code of Conduct in place yet? I thought it was due by now.	delete reply
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Anonymous wrote (29th May, 2010) I'm a CRC with an university research department, and we have just successfully won a renewal of our project grant. The problem is, my HOD now plans to siphon off the money from our project to run other unfunded projects - all my carefully planned budget is now in disarray and I will have to cut staff. Does this happen everywhere?	delete reply
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Anonymous wrote (12th May, 2010) Can anyone share how they communicate end of study results to the participants? And how do you make sure this happens, especially when final study results are often long after study personnel have gone on to new projects.	delete reply
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Anonymous wrote (27th Apr, 2010) The 20th May 2010 is the International Clinical Trials Day.	delete reply
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Anonymous wrote (9th Apr, 2010) Does the IRB-ethics committee from your site supply lists of its members to investigators?	delete reply
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Anonymous wrote (9th Apr, 2010) Is there a standard requirement for calibrating basic hospital equipment being used in clinical trials? Things like scales, thermometers, pulse oximeters, sphygmomanometers?	delete reply
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Anonymous wrote (4th Apr, 2010)

Some good discussion on the potential problems from stopping trials early due to good results in the latest JAMA. A study of over 100 trials asserts that in many of the trials the early positive effect would have diminished if the trial had been run to completion.

Anonymous wrote (30th Jan, 2010) I'm sure everyone has seen Wakefield all over the news with the GMC finding of misconduct over the MMR/autism research. Unbelievable that someone would pay kids at a birthday party for blood samples!	delete reply
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Anonymous wrote (21st Jan, 2010) DIA Annual European Meeting coming up soon, Monaco March 8-10.	delete reply
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Anonymous replied: (14th Apr, 2010)

Anyone go to this? Love to hear some feedback.

Anonymous wrote (7th Oct, 2009) Has anyone heard an update on the FDA/EMEA collaboration to improve GCP? I heard some stuff earlier this year about streamlining for GCP inspections etc.	delete reply
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