This webinar will examine the existing and proposed requirements for the FDA's DHF - including its derivative documents, the DMR and DHR. It will consider the MDD's TF/DD requirements, and evaluate the documents' differing purposes / goals. Required and desirable contents will be discussed.
business, education, science & technology
rules / e-learning / best practices / regulatory standards / quality system standards / fda regulation / hazard analysis trainings / hazard analysis training
Not specified
Public (what does this mean?)