icerat
Philosopher
While drug creation is a complex process, determining the effectiveness of a drug in human trials is a straight forward procedure that any doctor should be capable of preforming.
It depends on the drug, but in general, no it's not. In this case we're talking about treating brain cancers. The average doctor wouldn't even have the knowledge to assess progress, let alone the equipment.
Just because it doesn't follow the formal protocols established by today's practices doesn't mean it is ineffective or not a valid way of conducting research.
Correct. It's an ineffective and invalid way of conducting research because it wouldn't work.
We would know if a doctor prescribed it properly etc.. etc.. etc.. because he would be following the manufacturers guidelines and issuing his reports in a standardized format.
There are no manufacturer's guidelines for use of the drug in treating cancer. Research is what develops those guidelines
There is no reason why such standardized reports could not be created and issued to doctors who volunteer to engage in research of the drug.
Who would be issuing these standardized reports? In your "protocol" there's not even an overseeing team. Just a bunch of doctor's who for some reason are individually testing a drug. Who coordinated it? Who developed the protocols and experimental design? Who collected, collated, and analysed the data?
Where do they come from? On loan from a society with government funded research?