Please use this identifier to cite or link to this item:
https://www.um.edu.mt/library/oar/handle/123456789/145549| Title: | Compliance in quality control reviewing processes of finished products |
| Authors: | Galea, Claudia-Angélè Sammut Bartolo, Nicolette |
| Keywords: | Pharmaceutical industry -- Quality control Pharmacy -- Quality control Drugs -- Standards Pharmaceutical industry -- Documentation -- Standards Pharmaceutical industry -- Risk management |
| Issue Date: | 2026 |
| Publisher: | University of Malta. Department of Pharmacy |
| Citation: | Galea, C.A., & Sammut Bartolo, N. (2026). Compliance in quality control reviewing processes of finished products. Poster session presented at the 15th World Meeting on Pharmaceutics, Biopharmaceutics, and Pharmaceutical Technology, Prague. |
| Abstract: | Introduction: ◦ Quality Control (QC) documentation must be reliable and accurate to make sound batch release decisions. ◦
It must be independently reviewed in a standardised manner to ensure reliable, quality-based decisions. Aim: ◦ To develop a tool as a checklist to assist in mitigating and reducing errors that may occur during the QC documentation reviewing process of chemical analysis of finished drug products which may impact quality, patient safety or regulatory compliance. |
| URI: | https://www.um.edu.mt/library/oar/handle/123456789/145549 |
| Appears in Collections: | Scholarly Works - FacM&SPha |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Compliance in quality control reviewing processes of finished products.pdf | 445.27 kB | Adobe PDF | View/Open |
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