Übersetzung für "Blood relation " (Englisch → Deutsch) :

look for new treatments for blood related disorders | research new treatment for blood-related disorders | analyze new methods to cure blood related disorders | research new treatments for blood related disorders

blood cell | blood corpuscle | cellular blood component | cellular component of blood

blood glucose | blood glucose level | blood sugar | blood sugar level

alcoholemia | blood alcohol concentration | blood alcohol content | blood alcohol level | level of alcohol in the blood | BA [Abbr.] | BAC [Abbr.] | BAL [Abbr.]

take and determine blood pressure | take and interpret blood pressure of a patient | take and analyse blood pressure | take and determine blood pressure of a patient

blood product storage requirements | blood storage conditions | blood product storage conditions | blood product storage prerequisites

blood transfusion [ blood bank | blood donor ]

blood cell | blood corpuscule

Federal Decree of 22 March 1996 on the Control of Blood, Blood Products and Transplants

This action covers the following applications: (a) EU Health Portal — public health website and its sub-sites Europe for patients, crisis communication, Journalist Prize and Youth Health; (b) Injury Data Base (IDB) and Health in Europe: Information and Data Interface (HEIDI) data tool; (c) HEIDI Wiki; (d) Health Emergency Diseases Information System (HEDIS), Medical Intelligence System (MedIsys), and Early Warning and Reporting project (EAR); (e) Health Emergency Operations Facility (HEOF) — Crisis intranet; (f) rapid alert system information exchange on health threats due to deliberate release of chemical, biological and radio-nuclear agents — RAS-BICHAT and rapid alert system for information exchange on incidents including chemical a ...[+++]gents — RAS-CHEM; (g) Platforms: data collection on actions on diet, physical activity and health; database for the European Alcohol and Health Forum (Alcohol Clearing House — ACH); Mental health compass: Forum-related document management system; NGO database; (h) applications relating to blood, cells and tissues and tobacco: annual data collection of serious adverse reactions or events relating to blood transfusion and cells/tissues transplantation (SARE); register of all the tissue banks in the EU accessible by competent authorities in the Member States; system for annual reporting on voluntary unpaid donation, obligatory annual reporting for the Member States; register of tobacco product testing establishments in the EU and register of tobacco warnings, text and pictures, accessible by competent authorities in the Member States, and register for EU coding system for human tissues and cells; (i) cross-border health care, prescription register, medicine register; and (j) cross-policy services for public health applications and systems.

This Directive lays down those technical requirements, which take account of Council Recommendation 98/463/EC of 29 June 1998 on the suitability of blood and plasma donors and the screening of donated blood in the European Community , Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use , Commission Directive 2003/94/EC of 8 October 2003 laying down the principles and guidelines of good manufacturing practice in respect of medicinal pro ...[+++]ducts for human use and investigational medicinal products for human use , Commission Directive 2004/33/EC of 22 March 2004 implementing Directive 2002/98/EC of the European Parliament and of the Council as regards certain technical requirements for blood and blood components , certain recommendations of the Council of Europe, the monographs of the European Pharmacopoeia, particularly in respect of blood or blood components as a starting material for the manufacture of proprietary medicinal products, recommendations of the World Health Organisation, as well as international experience in this field.

Blood and blood components imported from third countries, including those used as starting material or raw material for the manufacture of medicinal products derived from human blood and human plasma intended for distribution in the Community, should meet equivalent Community standards and specifications relating to a quality system for blood establishments as set out in this Directive.

This Directive lays down those technical requirements, which take account of Council Recommendation 98/463/EC of 29 June 1998 on the suitability of blood and plasma donors and the screening of donated blood in the European Community , Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use , Commission Directive 2004/33/EC of 22 March 2004 implementing Directive 2002/98/EC of the European Parliament and of the Council as regards certain te ...[+++]chnical requirements for blood and blood components , and certain recommendations of the Council of Europe.