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 ...

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.

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 ...

Researchers engaged in pharma research and development must adhere to current Good Laboratory Practice (cGLP) and Good Manufacturing Practice (cGMP) standard operating procedures. Such regulatory ...

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 ...

Support from the FDA, industry groups and automation suppliers is helping pharmaceutical companies break the batch habit in favor of a continuous approach to drug production. In November 2016, ...

A CCS is mandated by EU and US regulations and ICH guidelines to ensure product safety and compliance in pharmaceutical manufacturing. Key CCS elements include monitoring, validation, contamination ...

This course is an adaptation of our standard 1-day GMP course, designed specifically for laboratory staff who have unique, additional requirements laid out in GMP both in the European and USA ...

An FDA report has illuminated problems at Emergent BioSolution's Baltimore manufacturing site, where the CDMO recently had to scrap up to 15 million Johnson & Johnson ...

State Key Laboratory on Technologies for Chinese Medicine Pharmaceutical Process Control and Intelligent Manufacture has the following research output in the current window (1 October 2024 - 30 ...