QC laboratories perform a critical role in demonstrating pharmaceutical products are consistently manufactured, safe, potent, and pure. At the same time, the number of tests run by QC laboratories is ...

Analytical quality control refers to all those processes and procedures designed to ensure that the results of laboratory analysis are consistent, comparable, accurate and within specified limits.

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The development and release of pharmaceutical products require the use of modern, efficient, and adaptable analytical techniques to assure efficacy and patient safety. The growing interest in complex ...

With the publication of ICH Q2(R2) and ICH Q14, the modern Quality by Design (QbD) paradigm introduced by ICH Q8 for manufacturing has now been extended to Quality Control (QC). A life cycle and ...

Dublin, June 04, 2025 (GLOBE NEWSWIRE) -- The "FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control" has been added to ResearchAndMarkets.com's offering. Join our upcoming ...

Biotherapeutics require extensive characterization and quality control (QC) testing prior to product release. These tests are resource intensive, time-consuming, and require updating as manufacturing ...

South Carolina Based Facility Provides Global Center of Excellence for the Company MORRISTOWN, N.J. November 28, 2012 – Today, Capsugel announced it has doubled its laboratory capacity with the ...

Global Pharmaceutical Quality Control Market is valued at approximately USD 4.71 billion in 2023 and is anticipated to grow with a healthy growth rate of more than 12.21% over the forecast period 2024 ...

DUBLIN--(BUSINESS WIRE)--The "Quality Control Laboratory Compliance - cGMPs and GLPs Course (ONLINE EVENT: October 21-22, 2025)" has been added to ResearchAndMarkets.com's offering. Maintaining ...