• Blood handling
  • Haemovigilance and recall of blood components
  • Application for a Blood Handling Licence
  • List of licensed handlers of blood (Blood establishments)
  • Legislation for blood handling
  • Special authorisation for import and export and notification of import and export of blood components
• Handling of cells, tissues and organs
• Advanced therapies medicinal products

Legislation for blood handling  

01 August 10

European blood directives (2002/98/EC; 2004/33/EC; 2005/61/EC; 2005/62/EC) were adapted and entered into national legislation during 2005 and 2006.
 
Blood Act (RT² I, 2005, 13, 63) (consolidated text May 2005)
Medicinal Product Act (RT I 2010, 15, 77 ) (consolidated text April 2010)

Regulations available in Estonian:
Guidelines for preparation of blood components
Quality requirements, quality assurance and microbiological screening of blood components
Donor eligibility criteria
Haemovigilance and recall order
Immunohaematological testing order
Infectious diseases screening order