Good Engineering Practice or GEP is applied to engineering and technical activities to ensure that a company manufactures products of the required quality as expected by the Regulatory Authorities. Good Engineering Practices are to ensure that the engineering or software development methodology generates deliverables that support the requirements for qualification or validation in the pharmaceutical industry.
See also
- GxP
- Good Manufacturing Practice (GMP)
- Best practice
- American National Standards Institute (ANSI)
- Institute of Electrical and Electronics Engineers (IEEE)
- European Medicines Agency (EMEA)
- Food and Drug Administration (FDA)
- Ministry of Health, Labour and Welfare (Japan)
- Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S)
Sources
This is about standards for quality assurance For other uses see GXP GxP is a general term for Good Practice Quality guidelines Good Manufacturing Practice or GMP (also referred to as 'cGMP' or 'current Good Manufacturing Practice' is a term that is recognized worldwide for the control and management Best Practice is an idea that asserts that there is a technique, method process activity incentive or reward that is more effective at delivering a particular outcome than The Institute of Electrical and Electronics Engineers or IEEE (read eye-triple-e) is an international Non-profit, professional organization The European Medicines Agency ( EMEA) is a European agency for the evaluation of medicinal products. The is one of Cabinet level ministries in the Japanese government. The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S are two international instruments between countries and pharmaceutical inspection authoritiesDapyx Software network: MP3 Explorer | Ebook Manager | Zenithic