{"id":503,"date":"2024-04-25T15:47:17","date_gmt":"2024-04-25T15:47:17","guid":{"rendered":"http:\/\/annualreport-2025.guerillainteractive.co.uk\/?page_id=503"},"modified":"2026-06-20T11:56:26","modified_gmt":"2026-06-20T11:56:26","slug":"table-of-abbreviations","status":"publish","type":"page","link":"https:\/\/annualreport.edqm.eu\/en\/table-of-abbreviations\/","title":{"rendered":"Table of abbreviations"},"content":{"rendered":"\t\t
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Table of abbreviations<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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TERM<\/strong><\/th>DESCRIPTION<\/strong><\/th>\n<\/tr>\n<\/thead>\n
3R principles<\/td>replacement, reduction and refinement (animal testing)<\/td>\n<\/tr>\n
AI<\/td>artificial intelligence<\/td>\n<\/tr>\n
AMA<\/td>African Medicines Agency<\/td>\n<\/tr>\n
AMQF<\/td>African Medicines Quality Forum<\/td>\n<\/tr>\n
AMRH<\/td>African Medicines Regulatory Harmonisation<\/td>\n<\/tr>\n
ANSM<\/td>French National Agency for Medicines and Health Products Safety (Agence nationale de s\u00e9curit\u00e9 du m\u00e9dicament et des produits de sant\u00e9)<\/td>\n<\/tr>\n
API<\/td>active pharmaceutical ingredient<\/td>\n<\/tr>\n
ASMF<\/td>Active Substance Master File<\/td>\n<\/tr>\n
ATD<\/td>anti-tampering device<\/td>\n<\/tr>\n
B-MJV<\/td>Blood Mutual Joint Visit<\/td>\n<\/tr>\n
B-PTS<\/td>Blood Proficiency Testing Scheme<\/td>\n<\/tr>\n
B-QM<\/td>Blood Quality Management Programme<\/td>\n<\/tr>\n
BRP<\/td>biological reference preparation<\/td>\n<\/tr>\n
BSP<\/td>Biological Standardisation Programme<\/td>\n<\/tr>\n
B-TES<\/td>Blood Tailored Expert Support<\/td>\n<\/tr>\n
B-TV<\/td>Blood Training Visit<\/td>\n<\/tr>\n
CAP<\/td>centrally authorised product<\/td>\n<\/tr>\n
CAS number<\/td>Chemical Abstracts Service Registry number<\/td>\n<\/tr>\n
CD-P-COS<\/td>European Committee for Cosmetics and Consumer Health<\/td>\n<\/tr>\n
CD-P-MCA<\/td>European Committee for Food Contact Materials and Articles<\/td>\n<\/tr>\n
CD-P-PH<\/td>European Committee on Pharmaceuticals and Pharmaceutical Care<\/td>\n<\/tr>\n
CD-P-PH\/CMED<\/td>Committee of Experts on Minimising the Public Health Risks Posed by Falsification of Medical Products and Similar Crimes<\/td>\n<\/tr>\n
CD-P-PH\/PC<\/td>Committee of Experts on Quality and Safety Standards in Pharmaceutical Practices and Pharmaceutical Care<\/td>\n<\/tr>\n
CD-P-PH\/PHO<\/td>Committee of Experts on the Classification of Medicines as Regards their Supply<\/td>\n<\/tr>\n
CD-P-TO<\/td>European Committee on Organs, Tissues and Cells<\/td>\n<\/tr>\n
CD-P-TS<\/td>European Committee on Blood Transfusion<\/td>\n<\/tr>\n
CEP<\/td>Certificate of Suitability to the European Pharmacopoeia monographs<\/td>\n<\/tr>\n
CLP<\/td>Regulation (EC) No 1272\/2008 on classification, labelling and packaging of substances and mixtures<\/td>\n<\/tr>\n
COS MSS<\/td>cosmetics market surveillance study<\/td>\n<\/tr>\n
COS PTS<\/td>cosmetics proficiency testing scheme<\/td>\n<\/tr>\n
COVID-19<\/td>coronavirus disease<\/td>\n<\/tr>\n
CRS<\/td>chemical reference substance<\/td>\n<\/tr>\n
DCD<\/td>donation after circulatory death<\/td>\n<\/tr>\n
DCP<\/td>decentralised procedure<\/td>\n<\/tr>\n
DG SANTE<\/td>Directorate General for Health and Food Safety<\/td>\n<\/tr>\n
DMF<\/td>Drug Master File<\/td>\n<\/tr>\n
DNA<\/td>deoxyribonucleic acid<\/td>\n<\/tr>\n
EAHP<\/td>European Association of Hospital Pharmacists<\/td>\n<\/tr>\n
ECHA<\/td>European Chemicals Agency<\/td>\n<\/tr>\n
EDA<\/td>Egyptian Drug Authority<\/td>\n<\/tr>\n
EDD<\/td>European Donation Day<\/td>\n<\/tr>\n
EDQM<\/td>European Directorate for the Quality of Medicines & HealthCare<\/td>\n<\/tr>\n
EDSForm<\/td>European Drug Shortages Formulary<\/td>\n<\/tr>\n
EDSForm WP<\/td>European Drug Shortages Formulary Working Party<\/td>\n<\/tr>\n
EEA<\/td>European Economic Area<\/td>\n<\/tr>\n
EFSA<\/td>European Food Safety Authority<\/td>\n<\/tr>\n
EFTA<\/td>European Free Trade Association<\/td>\n<\/tr>\n
EHMA<\/td>European Health Management Association<\/td>\n<\/tr>\n
EMA<\/td>European Medicines Agency<\/td>\n<\/tr>\n
EPC<\/td>European Pharmacopoeia Commission<\/td>\n<\/tr>\n
ESCP<\/td>European Society of Clinical Pharmacy<\/td>\n<\/tr>\n
EU<\/td>European Union<\/td>\n<\/tr>\n
FIP<\/td>International Pharmaceutical Federation<\/td>\n<\/tr>\n
GEON<\/td>General European OMCL Network<\/td>\n<\/tr>\n
GMP<\/td>good manufacturing practice<\/td>\n<\/tr>\n
HBc<\/td>hepatitis B core antigen<\/td>\n<\/tr>\n
HBsAg<\/td>hepatitis B surface antigen<\/td>\n<\/tr>\n
HCV<\/td>hepatitis C virus<\/td>\n<\/tr>\n
HIV<\/td>human immunodeficiency virus<\/td>\n<\/tr>\n
HMA<\/td>Heads of Medicines Agencies<\/td>\n<\/tr>\n
HMA-WGEO<\/td>EU Heads of Medicines Agencies\u2019 Working Group of Enforcement Officers<\/td>\n<\/tr>\n
HTS<\/td>high-throughput sequencing (see also NGS)<\/td>\n<\/tr>\n
HZJZ<\/td>Hrvatski zavod za javno zdravstvo
\nCroatian Institute of Public Health<\/td>\n<\/tr>\n
IgG<\/td>immunoglobulin<\/td>\n<\/tr>\n
IPC<\/td>Indian Pharmacopoeia Commission<\/td>\n<\/tr>\n
IR<\/td>infrared<\/td>\n<\/tr>\n
ISA<\/td>International Standards for Antibiotics<\/td>\n<\/tr>\n
ISBT<\/td>International Society of Blood Transfusion<\/td>\n<\/tr>\n
IVDR<\/td>Regulation (EU) 2017\/746 on in vitro diagnostic medical devices<\/td>\n<\/tr>\n
JP<\/td>Japanese Pharmacopoeia<\/td>\n<\/tr>\n
LAL<\/td>limulus amoebocyte lysate<\/td>\n<\/tr>\n
LNA<\/td>Laboratory of Dutch Pharmacists (Farmaceutisch Laboratorium)<\/td>\n<\/tr>\n
LNP<\/td>lipid nanoparticle<\/td>\n<\/tr>\n
mAb<\/td>monoclonal antibody<\/td>\n<\/tr>\n
MAT<\/td>monocyte-activation test<\/td>\n<\/tr>\n
MDR<\/td>Regulation (EU) 2017\/745 on medical devices<\/td>\n<\/tr>\n
MJA<\/td>Mutual Joint Audit<\/td>\n<\/tr>\n
MJV<\/td>Mutual Joint Visit<\/td>\n<\/tr>\n
mRNA<\/td>messenger ribonucleic acid<\/td>\n<\/tr>\n
MRP<\/td>Mutual Recognition Procedure<\/td>\n<\/tr>\n
MSS<\/td>market surveillance study<\/td>\n<\/tr>\n
NAT<\/td>nucleic amplification technique<\/td>\n<\/tr>\n
NCA<\/td>national competent authority<\/td>\n<\/tr>\n
NETTA<\/td>Network of National Focal Points on Travel for Transplantation<\/td>\n<\/tr>\n
NFP<\/td>national focal point<\/td>\n<\/tr>\n
NGS<\/td>next-generation sequencing (see also HTS)<\/td>\n<\/tr>\n
NOMA<\/td>Norwegian Medical Products Agency<\/td>\n<\/tr>\n
NPA<\/td>national pharmacopoeia authority<\/td>\n<\/tr>\n
OCABR<\/td>Official Control Authority Batch Release<\/td>\n<\/tr>\n
OCCL<\/td>official cosmetics control laboratory<\/td>\n<\/tr>\n
OMCL<\/td>official medicines control laboratory<\/td>\n<\/tr>\n
ONT<\/td>Organizaci\u00f3n Nacional de Trasplantes (Spanish National Transplant Organisation)<\/td>\n<\/tr>\n
PaedF WP<\/td>Euroepan Paediatric Formulary Working Party <\/td>\n<\/tr>\n
PaedForm<\/td>European Paediatric Formulary <\/td>\n<\/tr>\n
PDG<\/td>Pharmacopoeial Discussion Group<\/td>\n<\/tr>\n
PDMP<\/td>plasma-derived medicinal product<\/td>\n<\/tr>\n
Ph. Eur.<\/td>European Pharmacopoeia<\/td>\n<\/tr>\n
PTS<\/td>Proficiency Testing Scheme<\/td>\n<\/tr>\n
rFC<\/td>recombinant factor C<\/td>\n<\/tr>\n
RITTA<\/td>Registry of International Travel for Transplantation Activity<\/td>\n<\/tr>\n
RPT<\/td>rabbit pyrogen test<\/td>\n<\/tr>\n
RTEMIS<\/td>Real-Time Remote Inspection System<\/td>\n<\/tr>\n
SoHO<\/td>substance of human origin<\/td>\n<\/tr>\n
TFDA<\/td>Taiwan Food and Drug Administration<\/td>\n<\/tr>\n
TNF<\/td>tumour necrosis factor<\/td>\n<\/tr>\n
TOC<\/td>total organic carbon<\/td>\n<\/tr>\n
TV<\/td>training visit<\/td>\n<\/tr>\n
USP<\/td>United States Pharmacopeia<\/td>\n<\/tr>\n
UV<\/td>ultraviolet<\/td>\n<\/tr>\n
VBRN<\/td>Veterinary Batch Release Network<\/td>\n<\/tr>\n
WG<\/td>working group<\/td>\n<\/tr>\n
WHO<\/td>World Health Organization<\/td>\n<\/tr>\n
WP<\/td>working party<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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