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CEN CWA 149244WORKSHOPMarch 2004AGREEMENT
ICS 03.100.99English version European Guide to good Practice in Knowledge Management Part 4: Guidelines for Measuring KM
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What is european guide to good?
The European Guide to Good Manufacturing Practice (GMP) is a set of quality assurance standards for the pharmaceutical industry in Europe.
Who is required to file european guide to good?
All pharmaceutical companies operating in Europe are required to follow and comply with the European Guide to Good Manufacturing Practice (GMP) standards.
How to fill out european guide to good?
The European Guide to Good Manufacturing Practice (GMP) provides detailed guidelines on various aspects of pharmaceutical manufacturing, including quality control, production, and documentation. Companies can refer to these guidelines to ensure compliance.
What is the purpose of european guide to good?
The main purpose of the European Guide to Good Manufacturing Practice (GMP) is to ensure that pharmaceutical products are consistently produced and controlled according to quality standards. It aims to minimize the risks involved in pharmaceutical production and ensure the safety, efficacy, and quality of medicinal products.
What information must be reported on european guide to good?
The European Guide to Good Manufacturing Practice (GMP) does not specify specific information to be reported. However, it sets out general guidelines for quality assurance, documentation, and production controls that companies must adhere to.
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