RT Journal Article
SR Electronic
T1 How One Might Experimentally Determine if Container Closure Systems and their Components and Materials of Construction Contribute Elemental Impurities to Packaged Pharmaceutical Drug Products
JF PDA Journal of Pharmaceutical Science and Technology
JO PDA J Pharm Sci Technol
FD Parenteral Drug Association (PDA)
SP pdajpst.2018.008938
DO 10.5731/pdajpst.2018.008938
A1 Jenke, Dennis
YR 2018
UL http://journal.pda.org/content/early/2018/08/29/pdajpst.2018.008938.abstract
AB The safety aspects of elemental impurities in finished drug products is a topic of considerable importance in the pharmaceutical community and guidelines such as ICH Q3D and USP <232> and <233> have been published to provide directions on how to assess finished drug products with respect to such impurities. Although a drug product's packaging system has been identified as a potential source of elemental impurities, comparable guidelines have not been established for assessing packaging systems, and their materials and components of construction, with respect to their potential to contribute leached elements to packaged drug products. In this Commentary, the author considers the critical questions associated with selecting materials and components of construction and qualifying components and packaging with respect to their potential to add elemental impurities to packaged products and suggests means for accomplishing this objective.