Those responsible for the design, development and qualification of medical packaging, including medical devices, pharmaceuticals, in vitro diagnostics and biotechnology, to name a few key sectors, have a daunting challenge to achieve compliance with the general health and safety requirements put forth by the U.S. Food & Drug Administraton Code of Federal Regulations Title 21 CFR, Parts 800 to 1299. Adding sustainable packaging goals to that requirement list leads many of us to take the path of least resistance and shove sustainable packaging to the bottom of the list.
As the sustainable technology movement continues to grow, mature and become intrinsic to the business process, the medical technology sector is being tasked to incorporate sustainable technologies across its various sectors, with packaging being a huge target.
