Informed consent (IC) is a crucial issue in pharmacogenomics. IC is defined both as the printed signed document that is kept on record as well as the process of informing subjects about their ...
The author discusses the collection and evaluation of data part of FDA’s definition of process validation. Process validation is more than just running three consecutive batches under manufacturing ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback