cGMPs and Compliance Resource Center
Validation, calibration and qualification are extremely critical in pharmaceutical processes. Understanding them is necessary in order to meet cGMP guidelines.
Hyderabad-based API provider Neuland Labs sheds the stigma of Indian manufacturers by building stringent quality control into every process
Are the risks of leveraging this new technology outweighing the benefits for drug makers?
Industry standards help guide process instrument selection in pharmaceutical and biotech manufacturing environments, but further judgment is often required
White Papers: In Depth Research
Solutions Update: Quality, Compliance, Regulatory and Risk Management Solutions for the Increasingly Complex Pharmaceutical Industry
Posted: Sep 02, 2014
While market globalization has opened opportunities for pharmaceutical manufacturers, it has also intensified competition and the pressure to produce faster and at a lower cost.
Posted: Jul 30, 2014
Posted: Jul 29, 2014
Posted: Jul 14, 2014