I was just reading through Mason14's paper (which as many have stated, I also think is a great piece of work) and it raised a question around preclinical/ clinical trial design, and if it is common practise to involve a, or several, large pharma companies in the process?
Without discussing RAC specifically, I was wondering if Dr. T might shed any light on whether to his knowledge, this is common practise in such instances?
Equally, is there a consultation process with the FDA and other governing bodies around trial design, or are they simply presented with a road map once the company has finalised it?
Again, I'm not looking for info on RAC, more a better understanding of common practise.
Apologies if this has been covered.
I was just reading through Mason14's paper (which as many have...
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