Abkürzungen im GDP-Umfeld - Erweiterte Liste

Seminarempfehlung
Monday, 3 November 2025 14.00 - 16.00 h
A reliable Basis for Qualifying Service Providers?
Während der von CONCEPT HEIDELBERG bzw. der ECA organisierten GDP-Seminare kam mehrfach der Wunsch auf, eine Liste der im GDP-Umfeld verwendeten Abkürzungen zusammenzustellen. Die vor einigen Monaten erstmals veröffentlichte Übersicht wurden nun erweitert.
Allgemeine Abkürzungen
| 3PL | Third Party Logistics | 
| AMG | Arzneimittelgesetz | 
| AMWHV | Arzneimittel- und Wirkstoffherstellungsverordnung | 
| API | Active Pharmaceutical Ingredient (Wirkstoff) | 
| CAPA | Corrective and Preventive Actions (Korrektur- und Vorbeugemaßnahme) | 
| CC | Change Control | 
| CCP | Critical Control Point | 
| CFR | Code of Federal Regulations (Sammlung der Bundesverordnungen in den USA) | 
| CGMP | Current Good Manufacturing Practices | 
| CMO | Contract Manufacturing Organization | 
| COA | Certificate of Analysis (Analysenzertifikat) | 
| CRT | Controlled Room Temperature | 
| CSV | Computer System Validation | 
| DQ | Design Qualification (Designqualifizierung) | 
| DSCSA | Drug Supply Chain Security Act (USA) | 
| EEA | European Economic Area (Europäischer Wirtschaftsraum) | 
| EP | European Pharmacopoeia (Europäisches Arzneibuch) | 
| ERP | Enterprise Resource Planning | 
| EU | Europäische Union | 
| EWR | Europäischer Wirtschaftsraum | 
| FD&C Act | (U.S.) Food, Drug and Cosmetic Act | 
| FEFO | First Expiry First Out | 
| FIFO | First In First Out | 
| FMEA | Failure Mode and Effects Analysis | 
| GDP | Good Distribution Practice (Gute Vertriebspraxis) | 
| GMP | Good Manufacturing Practices (Gute Herstellungspraxis) | 
| GSP | Good Storage Practice (Gute Lagerpraxis) | 
| HACCP | Hazard Analysis and Critical Control Points | 
| IMP | Investigational Medicinal Product | 
| IQ | Installation Qualification (Installationsqualifizierung) | 
| KPI | Key Performance Indicator | 
| LIFO | Last In First Out | 
| MAA | Marketing Authorisation Application (Antrag auf Marktzulassung) | 
| MAH | Marketing Authorisation Holder (Zulassungsinhaber) | 
| MIA | Manufacture and Import Authorisation (Herstellungs- und Einfuhrerlaubnis) | 
| OOS | Out-of-Specification | 
| OQ | Operational Qualification (Funktionsqualifizierung) | 
| OTC | Over-the-Counter (rezeptfreies Arzneimittel) | 
| Ph. Eur. | Europäisches Arzneibuch | 
| PQ | Performance Qualification (Leistungsqualifizierung) | 
| PZN | Pharmazentralnummer | 
| QA | Quality Agreement (Qualitätsvereinbarung) | 
| QA | Quality Assurance (Qualitätssicherung) | 
| QC | Quality Control (Qualitätskontrolle) | 
| QK | Qualitätskontrolle | 
| QM | Qualitätsmanagement | 
| QMS | Qualitätsmanagementsystem | 
| QP | Qualified Person (Sachkundige Person) | 
| QRMS | Quality and Risk Management System (Qualitätsrisikomanagement) | 
| QSV | Qualitätssicherungsvereinbarung | 
| RA | Risk Analysis (Risikoanalyse) | 
| RP | Responsible Person (Verantwortliche Person) | 
| SMF | Site Master File | 
| SOP | Standard Operating Procedure (Standardarbeitsanweisung) | 
| TTSPP | Time and Temperature Sensitive Pharmaceutical Products | 
| VP | Verantwortliche Person | 
| WDA | Wholesale Distribution Authorisation (Großhandelserlaubnis) | 
| WMS | Warehouse Management System (Lagerverwaltungssystem) | 
Behörden und Organisationen
| ANVISA | Agência Nacional de Vigilância Sanitária (Brasilien) | https://www.gov.br/anvisa/pt-br | 
| APIC | Active Pharmaceutical Ingredients Committee | www.apic.cefic.org | 
| DIN | Deutsches Institut für Normung | www.din.de | 
| ECA | European Compliance Academy | www.gmp-compliance.org/ | 
| EDQM | European Directorate for the Quality of Medicines & HealthCare | www.edqm.eu/en/ | 
| EMA | European Medicines Agency (Europäische Arzneimittel-Agentur) | www.ema.europa.eu | 
| FDA | U.S. Food and Drug Administration | www.fda.gov/ | 
| GDPA | European GDP Association | www.good-distribution-practice-group.org/ | 
| HSA | Health Sciences Authority (Singapur) | https://www.hsa.gov.sg/ | 
| IATA | International Air Transport Association | https://www.iata.org/ | 
| ICH | International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use | www.ich.org/ | 
| IPEC | International Pharmaceutical Excipients Council | www.ipec-europe.org | 
| ISO | International Organization for Standardization | www.iso.org/ | 
| ISPE | International Society for Pharmaceutical Engineering | www.ispe.org | 
| MFDS | Ministry of Food and Drug Safety (Korea) | https://www.mfds.go.kr/ | 
| MHRA | Medicines and Healthcare products Regulatory Agency (Großbritannien) | www.gov.uk/government/organisations/medicines-and-healthcare-products-regulatory-agency | 
| PDA | Parenteral Drug Association | www.pda.org/ | 
| PIC/S | Pharmaceutical Inspection Co-operation Scheme | www.picscheme.org | 
| SFDA | Saudi Food and Drug Authority | https://www.sfda.gov.sa | 
| Swissmedic | Swiss Agency for Therapeutic Products (Schweizerisches Heilmittelinstitut) | https://www.swissmedic.ch | 
| TITCK | Turkish Medicines and Medical Devices Agency | https://www.titck.gov.tr/ | 
| USP | United States Pharmacopeia | www.usp.org | 
| WHO | World Health Organization (Weltgesundheitsorganisation) | www.who.int | 




