This week is simulation week and our project is on Bottle Label Development for a Hydrophilic Coating Product. This got me thinking about package development for products and the types of test they must pass. Any testing done on the packages should measure the effects and interactions of the levels of packaging, the package contents, external forces, and end-use. The testings usually involve controlled laboratory experiments in which documentation is very important. If you have any experience or know about the process that goes behind package development for medical devices, my question for you is: what are some examples of testings done and how was the procedure documented?