Developments in international/European health law

European Journal of Health Law

Volumn 16, Issue 1, 2009, Pages 81-88

  Abbing, Henriette D C Roscam ^a  

^a Department of Health Law ^*  (Netherlands)

Author keywords

Cross border health care; Medical research involving human subjects; Organ transplantation; Public communication on medicinal products

Indexed keywords

EUROPEAN UNION; HEALTH LEGISLATION; HUMAN; LAW; MEDICAL ETHICS; MEDICAL RESEARCH; ORGAN TRANSPLANTATION; PATIENT RIGHT; PROTECTION; QUALITY CONTROL; RESEARCH SUBJECT; SAFETY; SHORT SURVEY; STANDARD; ARTICLE; EUROPE; HEALTH CARE DELIVERY; HUMAN EXPERIMENT; INTERNATIONAL COOPERATION; LEGAL ASPECT;

BIOMEDICAL RESEARCH; DELIVERY OF HEALTH CARE; EUROPE; HEALTH SERVICES ACCESSIBILITY; HUMAN EXPERIMENTATION; HUMANS; INTERNATIONAL COOPERATION; ORGAN TRANSPLANTATION; PATIENT RIGHTS;

EID: 66149149502     PISSN: 09290273     EISSN: 15718093     Source Type: Journal    
DOI: 10.1163/157180909X400240     Document Type: Short Survey

References (17)

1. The text can be found on the relevant section of the ec.europa.eu website and through the European Public Health Portal.
2. Henrietxe D. C. Roscam Abbing. New developments in international health law EJHL, 1998, p. 160-161.
3. Directive 2002/98/EC setting standards of quality and safety for the collection, testing, storage and distribution of human blood and blood components, PB L 33 of 8.2. 2003, p. 30; Directive 2004/23/EC setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells, PB L102 of 7.4. 2004, p. 48.
4. Article 13
5. Member states shall ensure that donations of human organs from deceased and living donors are voluntary and unpaid;
6. Member states shall prohibit advertising the need for or, availability of, human organs where such advertising has a view to offering or seeking financial gain or comparable advantage;
7. Member States shall ensure that the procurement of organs is carried out on a non-profit basis. Blood Directive, article 20: Member states shall take the necessary measures encouraging -. Tissues and Cells Directive, article 12: member states shall endeavour to ensure voluntary etc.
8. Directive 2004/33 implementing Directive 2002/98/EC.
9. Annex to Directive 2004/23.
10. Such as Eurotransplant International and Scandiatransplant.
11. L. Gevers, A fair distribution of organs for transplantation purposes: looking to the past and the future. EJHL 2007, 215-219. (Pubitemid 350059068)
12. Henriette D. C. Roscam Abbing, A Council of Europe Protocol on Transplantation of Organs and Tissues of Human Origin EJHL, 2002, 63-76. (Pubitemid 34650898)
13. The text can be found on the relevant section of the ec.europa.eu website and through the European Public Health Portal.
14. Insured persons: until the date of application of Regulation no 883/2004 a person who is insured in accordance with the provision of articles 1, 2, and 4 of Regulation (EC) 1408/71; as from the date of its application article lc of Regulation no 883/2004.
15. This includes care without overnight accommodation requiring high specialised and cost-intensive infrastructure or medical requirement or care involving treatment presenting a particular risk. These situations will be specified on a list by the Commission.
16. The text can be found on the relevant section of the ec.europa.eu website (enterprise and industry).
17. For products authorised in accordance with regulation 726/2004, certain approval tasks are given to the European Medicinal Agency.