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Wakankar, A.A., Wang, Y.J., Canova-Davis, E., Ma, S., Schmalzing, D., Grieco, J., et al. (2010) On Developing a Process for Conducting Extractable-Leachable Assessment of Components Used for Storage of Biopharmaceuticals. Journal of Pharmaceutical Sciences, 99, 2209-2218.
https://doi.org/10.1002/jps.22012

has been cited by the following article:

• TITLE: Strengthening Extractable & Leachable Study Submissions: Best Practices to Avoid Regulatory Deficiencies

  AUTHORS: Subathra Ramamoorthy, Ngee Sing Chong, Kishore Kumar Hotha

  KEYWORDS: Extractables and Leachables, Pharmaceutical Container Closure Systems, Manufacturing Equipment, Guidance, Regulatory Standards, Prototype Procedures

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.15 No.12, December 26, 2024

  ABSTRACT: The assessment of extractable and leachables (E&L) has become a cornerstone of pharmaceutical product safety, yet no unified global standards currently exist to quantify or report E&L from container closure systems. While initially limited to primary packaging, E&L evaluations now encompass secondary packaging, manufacturing equipment, and medical devices. Key milestones include the FDA’s 1999 guidance on container closure systems and more recent frameworks from USP chapters , , and , as well as PQRI recommendations. These guidelines have set the foundation for conducting E&L studies, especially for high-risk dosage forms, and are complemented by the forthcoming ICH Q3E, which aims to standardize E&L considerations across dosage forms. This article outlines a structured procedure for E&L assessments, integrating regulatory expectations with practical insights.