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How do you write a quality agreement? Muhammad Asim Niazi
October 18, 2024
The quality agreement is a highly technical document between the pharma product owner and manufacturing contractor to ensure quality in each process and resultant final product.
Steam Quality and Testing Muhammad Asim Niazi
August 09, 2024
Steam quality testing determines the acceptability of steam for pharma applications and points out any shortcomings.
Digital Transformation in Pharmaceutical Quality Management Muhammad Asim Niazi
August 08, 2024
Digital transformation helps pharma organizations increase efficiency, speed, and accuracy in their quality operations.
Brief Summary of FDA Quality Management Maturity Program Muhammad Asim Niazi
March 05, 2024
United States FDA has a pivotal role in providing guidance for pharmaceutical quality attributes and defining new ways to improve the quality by publishing new regulations for quality enhancement.
Pharmaceutical Quality System Muhammad Asim Niazi
January 15, 2024
The quality of drug products is critical and integral for many Pharma manufacturers. It is the basis on which the relevant pharma controls, resources, activities, and growth are defined.
Quality by design (QbD) in bio manufacturing Shruti Talashi
December 01, 2023
Quality by design is the standard approach used for demonstrating and achieving consistent, high quality product. Rather than relying on just the post production testing, QbD practice rather encourages to improve quality at every stage of the process.
Top 5 Tips About Quality Control of Pharma Intermediates Production PharmaSources
November 17, 2023
In an industry where precision and accuracy are paramount, quality control and testing are guardians of pharmaceutical integrity, promoting the development of safe and effective medications.
Quality management system and Digitalization end-to-end process: Pharma 4.0 and Industry 4.0 Shruti Talashi
September 14, 2023
Drugs that are available in the market should not deviate from its standardized quality parameters.
Update on ICH Q9(R1) Quality Risk Management Muhammad Asim Niazi
August 23, 2023
In collaboration with the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use – ICH, the FDA has updated the 2006 version of Q9 Quality Risk Management.
Quality Sourcing Opportunities at 2022 Zhejiang Export Commodity Online Fair “Thailand & Indonesia - Natural Extracts Session”! PharmaSources.com
June 17, 2022
The 2022 Zhejiang Export Commodity Online Fair (Pharma Sector) is coming with a new session. The portals for the “Thailand & Indonesia - Natural Extracts Session” is now launched to welcome the participation of both pharmaceutical suppliers ...