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Terminology This glossary includes some of the terms and abbreviations used regularly in the pharmaceutical water and sterilisation arenas. We hope it will help should we unintentionally use jargon on this site. We have also included a number of internet links which will take you directly to the relevant website. If there are any other terms you feel would help please let us know and we will include them on our list. |
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API CCA cGMP CIP CIPSIP DQ EDI FMEA GAMP GCLP GMP HACCP HTM IQ LAL NDT OQ Ph Eur PLC PQ PTFE PW QA QC SIP SOP TIG TOC URS USP VMP WFI |
Active Pharmaceutical Ingredient Continuous Compliance Assurance Code of Federal Regulations Current Good Manufacturing Practice Clean in Place Clean and Steam in Place Design Qualification Electrodeionisation European Medicines Agency Food and Drug Administration Failure Modes and Effects Analysis Good Automated Manufacturing Practice Good Control Laboratory Practice Good Manufacturing Practice Hazard Analysis and Critical Control Points Health Technical Memorandum International Conference on Harmonisation Installation Qualification Irish Medicines Board Limulus Amoebocyte Lysate Medicines and Healthcare products Regulatory Agency (formerly MCA) Non Destructive Testing Operational Qualification European Pharmacopoeia Programmable Logic Controller Performance Qualification Polytetrafluroethylene Purified Water Quality Assurance Quality Control Steam in Place Standard Operating Procedure Tungsten Inert Gas Total Organic Carbon User Requirements Specification United States Pharmacopoeia Validation Master Plan Water for Injection World Health Organisation |
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