Traduction de «committee on blood safety » (Français → Néerlandais) :

Meeting of the Advisory Committee on Blood Safety & Availability (ACBSA), 30 May 2008: Clinical Significance of Red Cell Age in Transfusions; 2008 [accessed 2008 June 17].
Meeting of the Advisory Committee on Blood Safety & Availability (ACSBA), 30 May 2008: Clinical Significance of Red Cell Age in Transfusions; 2008 [accessed 2008 June 17].

7.3 RESEARCH QUESTIONS IMPROVING OPTIMAL BLOOD SAFETY______________________________35
7.3 RESEARCH QUESTIONS IMPROVING OPTIMAL BLOOD SAFETY______________________________34

and Antibacterial Properties of Riboflavin and Light: Applications To Blood Safety and Transfusion Medicine.
‐ Goodrich RP, Edrich RA, Goodrich LL, Scott CA, Manica KJ, Hlavinka DJ, et al. The Antiviral and Antibacterial Properties of Riboflavin and Light: Applications To Blood Safety and Transfusion Medicine.

Dans l’UE, il a été décidé à l’‘Adare Colloquium on Blood Safety and Self-sufficiency’, en 1996, que le dépistage ALT était devenu superflu.
In de EU werd op het ‘Adare Colloquium on Blood Safety and Self-sufficiency’ in 1996 besloten dat ALT screening overbodig geworden was.

Morbidity and mortalility weekly report Nucleic acid sequence based amplification Nucleic Acid Amplification Testing National Institute for Biological Standards and Control Occupational Safety and Health Administration Phosphate buffered saline ou tampon phosphate Polymerase chain reaction Stérilisation acide peracétique-éthanol Positive predictive value Polyvinyl-pyrrolidon Povidone-iodine Dérivés de l’ammonium quaternaire Ribonuclease H Reverse transcriptase ou transcriptase inverse Advisory Committee on the Safety of Blood, Tissues and Organs Sterility assurance level Severe acute respiratory syndrome Syndrome d’immunodéficience acquise Median tissue culture infective dose Test d’immunofluorescence indirecte Transcription-mediated amplification Tumor necrosis factor Test de radio-immunoprécipitation United Kingdom United Kingdom Blood Transfusion Services Ultraviolet Vapour-phase hydrogen peroxide Valeur prédictive positive Virus respiratoire syncytial Etats-Unis Werkgroep infectiepreventie ou groupe de travail sur la prévention des infections West Nile virus World Health Organization
Nucleic acid sequence based amplification Nucleic Acid Amplification Testing Non-heart beating donors National Institute for Biological Standards and Control Optische densiteit Occupational Safety and Health Administration Perazijnzuur Phosphate buffered saline Polymerase chain reaction Perazijnzuur ethanol sterilisatie Positive predictive value Positief predictieve waarde Polyvinyl-pyrrolidon Povidone-iodine Quaternaire ammoniumverbindingen Radio-immunoprecipitatie test Ribonucleic acid Ribonuclease H Respiratoir syncytiaal virus Reverse transcriptase Advisory Committee on the Safety of Blood, Tissues and Organs Sterility assurance level Severe acute respiratory syndrome Median tissue culture infective dose Transcription-mediated amplification Tumor necrosis factor United Kingdom United Kingdom Blood Transfusion Services Ultraviolet Vapour-phase hydrogen peroxide Verenigde Staten Werkgroep infectiepreventie West Nile virus World Health Organization

– SaBTO - Advisory Committee on the Safety of Blood, Tissues and Organs. Department of Health: Guidance on the microbiological safety of human organs, tissues and cells used in transplantation; 2011. internet: [http ...]
Health: Guidance on the microbiological safety of human organs, tissues and cells used in transplantation; 2011. internet: [http ...]

disease and blood screening tests» Current Opinion in Hematology, Vol. 11:351-356, 2004. l) Exposé « Modelling of effects of the exclusion of transfusion recipients» TSE - Safety
disease and blood screening tests» Current Opinion in Hematology, Vol. 11:351-356, 2004. l) Uiteenzetting « Modelling of effects of the exclusion of transfusion recipients» TSE -

DJA Pour les substances dont la dose journalière admissible (DJA) a été établie au niveau européen, les données provenant de l’EFSA (European Food Safety Authority), de l’EMEA (The European Agency for the Evaluation of Medical Products) ou du SCAN (Scientific Committee on Animal Nutrition) ont été prises en compte.
ADI Voor stoffen waarvoor de aanvaardbare dagelijkse opnames (ADI) is vastgesteld op Europees vlak werd rekening gehouden met de gegevens die afkomstig zijn van de EFSA (European Food Safety Authority), de EMEA (The European Agency for the Evaluation of Medical Products) of de SCAN (Scientific Committee on Animal Nutrition).

2002, 5 – 9; - , „Belgian standards for patient safety in Anesthesia. The Belgian Anesthesia Patient Safetyh Steering – Committee‰, Acta Anaesthesiol.
The Belgian Anesthesia Patient Safetyh Steering – Committee‰, Acta Anaesthesiol.

Cette position a été confirmée par le ‘FDA Blood Product Advisory Committee’ en mars 1995.
Dit werd bevestigd door het ‘FDA Blood Product Advisory Committee’ in maart 1995.