Manufacturing system validation in the pharmaceutical industry – EBR/MES system validation
System validation in the pharmaceutical industry is a crucial process to ensure that computerized systems are fit for their intended
System validation in the pharmaceutical industry is a crucial process to ensure that computerized systems are fit for their intended
In today’s world, businesses are increasingly facing pressure to operate in a sustainable and responsible manner. This is not only
The pharmaceutical industry is responsible for the development, production, and distribution of medicines and other healthcare products. In order to
Data integrity is the linchpin of pharmaceutical manufacturing under Current Good Manufacturing Practices (cGMP). It ensures that data generated throughout
In the pharmaceutical and manufacturing industries, Generic Master Batch Records (GMBRs) are increasingly being used to improve packaging efficiency. GMBRs
Manufacturers operating in the automotive industry are currently facing a major challenge – maintaining competitiveness while mitigating the environmental impact
Quality Inspections are automatic way for periodic quality tests with immediate confirmation if measurement is within quality limits. Measurements are
It’s no secret that every step of the pharmaceutical manufacturing process must be documented. However, managing paper documentation can be
SPC, or statistical process control, is one of the most interesting tools in the context of quality management. Nowadays,
Let’s be honest – the term “rework” is most commonly associated with delays in production. Technically speaking, rework means correcting
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