The European Commission’s new “rolling plan” for Medical Device Regulations and In Vitro Device Regulations came one step closer to being realized as key implementation deadlines were announced recently. This list of critical deadlines includes deadlines for various initiatives along with 12 implementing actions required for the new regulations to be put into place. Tap into essential information regarding the release of these deadlines, which comes as welcome news to an industry that was largely unaware of when this fundamental information for the implementation of new medical device and IVD regulations would become available.