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SIXTH FRAMEWORK Program PRIORITY: Structuring the European Research Area SCIENCE AND SOCIETY Contract for: SPECIFIC TARGETED RESEARCH PROJECT (STREP) From GMP to GBP Report of GBP survey WP 2, Final
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From GMP (Good Manufacturing Practice) to GBP (Good Distribution Practice) is the transition of regulatory standards in the pharmaceutical industry.
Companies involved in manufacturing and distributing pharmaceutical products are required to comply with the transition from GMP to GBP.
To fill out from GMP to GBP, companies must ensure their manufacturing and distribution processes align with the updated regulatory standards.
The purpose of transitioning from GMP to GBP is to ensure the safety, quality, and efficacy of pharmaceutical products throughout the supply chain.
Information related to manufacturing practices, distribution processes, quality control measures, and regulatory compliance must be reported during the transition from GMP to GBP.
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