Published: July 2025
Pages: 16
Effective complaint handling is critical for maintaining product integrity, safeguarding patient safety, and driving continual improvement.
This Standard Operating Procedure (SOP) includes a template that helps the user outline the process for receiving, documenting, evaluating, and resolving product quality complaints within the pharmaceutical organization. The purpose of the SOP is to ensure that all reported product quality issues are managed in a consistent, timely, and compliant manner in alignment with applicable regulatory requirements, such as the US Food and Drug Administration (FDA) 21 CFR, and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines.
Add all seven QMS SOP Templates to your cart and automatically unlock a 20% bundle purchase discount. View All
ISPE members located in nations with emerging economies* are eligible for a 50% discount on publications from the regular member price. To receive the discount, members must be logged in with their ISPE member account. Contact Member Services at ask@ispe.org for more information or if you have questions about your membership status or this discount program. Discounts do not apply to Accuris (formerly Techstreet) document downloads.
*Based on the World Bank's system for classifying national economies by GNI per capita. Includes low-income, lower middle-income, and upper middle-income economies. To learn more about the World Bank classification system, please click here. Currently includes the following nations, except where international sanctions apply: