Developing a Simplified Model Standard Operating Procedure to Implement Quality Metrics for Pharmaceutical Manufacturing System

Author:

Potdar Manohar,Hivrale Madhuri,Bhavare Neha,Thosar Rohan,Jagtap Supriya

Publisher

Springer Nature Singapore

Reference7 articles.

1. https://www.projectmanagementdocs.com/template/projectdocuments/quality-metricsaxzz6LSs7JVFo – Google Search [Internet]. [cited 2023 Apr 11]. Available from: https://www.google.com/search?q=te+https%3A%2F%2Fwww.projectmanagementdocs.com%2Ftemplate%2Fprojectdocuments%2Fqualitymetrics%2F%23axzz6LSs7JVFo&rlz=1C1ONGR_enIN1020IN1020&oq=te+https%3A%2F%2Fwww.projectmanagementdocs.com%2Ftemplate%2Fprojectdocuments%2Fquality-metrics%2F%23axzz6LSs7JVFo&aqs=chrome..69i57.9167j0j15&sourceid=chrome&ie=UTF-8

2. CDER/USFDA. Request for quality metrics guidance for industry request for quality metrics guidance for industry. 2015;(July):1–24. Available from: http://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm455957.pdf

3. Torkko M, Katajavuori N, Linna A, Juppo AM. The utilization of quality KPIs in the pharmaceutical industry. J Pharm Innov. 2014;9(3):175–82.

4. World Health Organization. Good manufacturing practices for sterile pharmaceutical products. WHO Tech Rep Ser. 2011;961:45–7.

5. Medicines Control Council. Guide to good manufacturing practice. 2010;4.01(June 2009):1–158.

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