As you surmised, in several instances, the FDA was relaxed
in detecting missing information, did not note severe problems,
or dismissed
professionals who noted the errors.
Throughout history, mistakes, false claims, and bad product lines -
along with loud objections and cries from the public - have led to
establishing new rules, amendments, and regulations.
But do these laws hold significant meaning for everyone?
As we saw in the special insert of the Rusnak
article regarding the
Washington Post article,
Fundamentals of
Clinical Trials - Lesson 1 - Topic 4 - Page 1 of 2
