I didn’t do my undergraduate at NJIT ,but I believe it’s common for a medical device to go through common steps. Those steps may just have a different name and ask for specific information. I think it’s good that they require the students in that course to have to do a test plan document. It often seems as though we think a product has to be perfect before it goes on the market , but it seems that it is not true; Due to the quality of different products. even though a company goes through all that paper work for a product. Is it really worth it in the end ? If the product does not perform at its best ability ? A medical device document will be even longer as we had seen in the sample documents that Dr. Simon has given us.