White paper: Validation and qualification
In a regulated environment
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The qualification of equipment in the pharmaceutical industry is a significant part of quality assurance and is required by law. This white paper provides an overview of how validation and qualification are classified in a GMP1 environment and describes the general approach for qualification with the key steps of DQ2, IQ3, OQ4, and PQ5. The focus is on unit qualification. The white paper also covers the validation of computer-based systems. The white paper is aimed primarily at interested parties who are yet to have looked into the topic of "validation and qualification."
Content of the white paper:
- Good manufacturing practice
- GMP publications by various organizations
- Types of validation
- Validation of computer-based systems
- Validated system