Category: Manufacturing

The Manufacturing category covers the processes, equipment, and controls that ensure pharmaceutical production meets GMP requirements.

Topics include raw material handling, granulation, packaging, process validation, cleaning validation, qualification activities, and risk-based approaches in line with EU GMP and FDA standards. Supporting areas such as environmental controls, batch records, and manufacturing documentation are also addressed.

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Quality Risk Management Process

Quality Risk Management in the Pharmaceutical Industry

Explore the essentials of Quality Risk Management in Pharma: Principles, tools, guidelines, and implementation strategies for enhanced safety....

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