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Discussion Board: Comments & Questions

Anonymous wrote (29th May, 2010) Has anyone been following the debate on Medscape - ''Why aren't doctors allowed to care about money?".	delete reply
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Anonymous wrote (15th Apr, 2010) Medical students do some strange research these days. Just saw a publication that looked at TV med dramas such as House and Greys Anatomy and concluded they were rife with ethical dilemmas and professional misconduct. No surprise there really! The other interesting finding was that over 80% of medical students watch the TV shows - where do they get the time!	delete reply
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Anonymous wrote (15th Apr, 2010) I see ACRP are looking for people to deliver on line seminars, they pay $250 for 90minutes. Has anyone done this?	delete reply
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Anonymous wrote (10th Mar, 2010) Is anyone going to the DIA meeting in Washington DC in June? Do any medicos go or is is all industry people?	delete reply
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Anonymous wrote (28th Feb, 2010) can suggestions on start up of a new research site. Aside from getting the site ready is there anything else	delete reply
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Anonymous wrote (28th Feb, 2010) Those of us doing medical device trials will be interested to see new FDA Guidance on acceptable statistical methods for combining data from multiple trials. Should make things a bit easier.	delete reply
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Anonymous wrote (26th Feb, 2010) The FDA has proposed a rule requiring sponsors to report information if they are aware of falsification of data. Open for submissions now.	delete reply
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Kathy Benish wrote (23rd Feb, 2010)

I have tried most of these things and still get "this is the budget and we are not willing to negotiate". Any suggestions on how to come up with a time frame for procedures? For an example: most Sponsors/CRO's say it should take up to an hr for the consent process. I almost laugh at this. If you go over the consent, do the explanations , have each page initialed and/or signed, copy the consent for the pt. and go over explaining all the procedures and what is expected it can take 2-3 hrs. How do you budget for this?

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Anonymous wrote (16th Feb, 2010) i want to talk about medical writers. i have read a lot lately about ghostwriting no longer being OK, but the reality is that many researchers are just not good writers! how are we suppsoed to communicate our results if we cant use writing professionals to help us write?	delete reply
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Anonymous wrote (13th Feb, 2010) Does anyone have any advice on whether it is worth going to the Liability Risks in Clinical Trials meeting in Washington on February 25, 2010? It's run by DIA.	delete reply
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