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. 2011 Aug 30;3:117–186. doi: 10.2147/CEOR.S14407

Table 2.

Comparison of processes for identifying, selecting, and assessing technologies

Country Centralized reimbursement review/decision-making body (role) Technologies to be considered for review
Health technology assessment
Technology identification Technology selection Synthesis and analysis of evidence (assessment report) Evaluation of evidence provided (evaluation report)
Austria
  • Association of Austrian Social Security Institutions (decisions)55

  • Pharmaceutical Evaluation Board (recommendations)56

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals58

  • Typically considered in order received58

  • Manufacturer through submission requirements55

  • Methods should comply with internationally recognized systematic review and economic guidelines55

  • Technical staff within Association of Austrian Social Security Institutions (Department of Pharmaceutical Affairs – pharmacological and medical-therapeutic assessment; Health Economics Team – economic assessment)55

Belgium
  • Minister of Social Affairs (decisions)

  • Commission on reimbursement of medicines/Drug Reimbursement Committee (CRM) (recommendations)9

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals17

  • Typically considered in order received17

  • Manufacturer through submission requirements9

  • Methods should comply with internationally recognized systematic review guidelines9

  • Technical staff within CRM supported by external experts9

Czech Republic
  • State Institute for Drug Control (decisions)65

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals66

  • Typically considered in order received65

  • Manufacturer through submission requirements66

  • Technical staff within State Institute for Drug Control65

Denmark
  • Danish Medicines Agency (decisions)68,69,121

  • Reimbursement Committee (recommendations)68,121

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals84

  • Typically considered in order received84

  • Manufacturer through submission requirements68

  • Methods must comply with “Danish guidelines for the socioeconomic analysis of medicines”68

  • Technical staff within Danish Medicines Agency supported by external experts, if necessary68

Estonia
  • Ministry of Social Affairs (decisions)72

  • Pharmaceuticals Committee (recommendations)72

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals72

  • Not specified

  • Manufacturer through submission requirements72

  • Technical staff within Estonian Health Insurance Fund and State Agency of Medicines72

Finland
  • Pharmaceuticals Pricing Board (decisions)73,74,76

  • Pharmaceuticals Pricing Board Expert Group (recommendations)75

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals76

  • Typically considered in order received73

  • Manufacturer through submission requirements122

  • Methods must comply with guidelines of the Ministry of Social Affairs and Health122

  • Technical staff within Pharmaceuticals Pricing Board supported by external experts122

France
  • Ministry for Health and Social Security (decisions)21,78

  • French National Authority for Health (recommendations)78

Depends on type of appraisal16,20
Single technology appraisal
Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals and devices

  • Health care professional associations seeking reimbursement for procedures

Multiple technology appraisals
Typically classes of pharmaceuticals or categories of devices
Referred by:
  • Health care professional associations

  • Ministry of Health

  • National Union of Health Insurance Funds

  • Patient and/or carer organizations120

Single technology appraisals
  • Typically considered in order received16

Multiple technology appraisals
  • Selection criteria not specified

Single technology appraisals
  • Manufacturer through submission requirements20

Multiple technology appraisals
  • Technical staff within Health and Social Security supported by external experts20

  • Methods should comply with internationally recognized systematic review and economic guidelines20

Single technology appraisals
  • Technical staff within Health and Social Security supported by external experts20

Multiple technology appraisals
  • Technical staff within Health and Social Security or independent academic group20

Germany
  • Federal Joint Committee (decisions)19

  • Institute for Quality and Efficiency in Health Care (recommendations)19

Referred by:
  • Associations represented by Federal Joint Committee

  • Ministry of Health

  • Institute for Quality and Efficiency in Health Care

  • Federal commissioner of patient affairs

  • Patient and/or carer organizations18

  • Determined by Federal Joint Committee

  • Selection criteria:
    1. Clinical relevance
    2. Cost implications
    3. “Risks”6
  • Technical staff within Institute for Quality and Efficiency in Health Care supported by external experts123,124

  • Methods must comply with Institute for Quality and Efficiency in Health Care systematic review and economic guidelines124

  • Technical staff within Institute for Quality and Efficiency in Health Care supported by external experts123,124

Greece
  • Transparency Committee in the Reimbursement and Medicinal Products (makes decisions)85

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals85

  • Not specified

  • Manufacturer through submission requirements85

  • Technical staff within Transparency Committee in the Reimbursement and Medicinal Products85

Hungary
  • Ministers of Health and Finance (decisions)

  • National Health Insurance Fund Administration (recommendations)88,89

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals

  • National Health Insurance Fund Administration88

  • Not specified

  • Technical staff within National Technology Assessment Office of the National Institute for Strategic Health Research90

  • Technical staff within National Technology Assessment Office of the National Institute for Strategic Health Research90

Ireland
  • Health Service Executive (decisions)91,92

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals91


Referred by:
  • Department of Health and Children of the Health Services Executive for new and existing devices and diagnostic tests that might “incur a high cost or have a significant budget impact”91

  • Not specified

  • Manufacturer through submission requirements93,125

  • Methods must comply with Irish Health Technology Assessment Guidelines93

  • Technical staff within National Centre for Pharmacoeconomics, supported by external clinical experts93

Italy
  • Italian Medicines Agency Technical Scientific Committee (decisions)94

  • Italian Medicines Agency Pricing and Reimbursement Committee (recommendations)95

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals27

  • Typically considered in order received27

  • Manufacturer through submission requirements126

  • Methods must comply with Italian submission guidelines27

  • Members of Technical Scientific Committee126

Norway
  • Norwegian Medicines Agency (decisions)98

  • Department of Pharmacoeconomics (recommendations)98

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals34

  • Not specified

  • Manufacturer through submission requirements34

  • Methods should comply with internationally recognized systematic review guidelines34

  • Technical staff within Norwegian Medicines Agency and Department of Pharmacoeconomics98

Poland
  • Ministry of Health (decisions)99

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals99

  • Not specified

  • Manufacturer through submission requirements99

  • Technical staff within Ministry of Health99

  • Agency for Health Technology Assessment127

Portugal
  • Ministry of Health (decisions)

  • INFARMED (recommendations)36,45

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals36

  • Not specified

  • Manufacturer through submission requirements36

  • Technical staff within INFARMED supported by external experts36

Scotland
  • National Health Service Scotland (decisions)30

  • Scottish Medicines Consortium (recommendations)

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals104

  • Automatic within 12 weeks of market launch104

  • Exclusion criteria: Already appraised by National Institute of Health and Clinical Excellence through its multiple technologies appraisal process104

  • Manufacturer through submission requirements128

  • Methods must comply with Scottish Medicines Consortium systematic review and economic guidelines34

  • Technical staff within Scottish Medicines Consortium supported by external experts128

Slovakia
  • Ministry of Health (decisions)

  • Reimbursement Committee for Medicinal Products (recommendations)105,107,129,106

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals104

  • Not specified

  • Manufacturer through submission requirements131

  • Working group for pharmacoeconomics and outcomes research131

Spain
  • Ministry of Health Directorate General of Pharmacy and Health Products

  • Inter-Ministerial Pricing Commission (decisions)21,108

Referred by:
  • Ministry of Health (newly approved pharmaceuticals)108

  • Not specified

  • Manufacturer through invitation to submit information to Inter-Ministerial Pricing Commission21

  • Technical staff within Ministry of Health132

  • Inter-Ministerial Pricing Commission21

Sweden
  • Dental and Pharmaceutical Benefits Board (decisions)15,109,110

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals104

  • Dental and Pharmaceutical Benefits Board (for pharmaceuticals approved prior to 2002)133,134

  • For new pharmaceuticals: typically considered in order received

  • For older pharmaceuticals: Overall sales volume134,135

  • For new pharmaceuticals: Manufacturer through submission requirements136

  • For older pharmaceuticals: Technical staff within Dental and Pharmaceutical Benefits Board supported by external experts136

  • Methods must comply with Dental and Pharmaceutical Benefits Board systematic review and economic guidelines10

  • For new pharmaceuticals: Technical staff within Dental and Pharmaceutical Benefits Board136

  • For older pharmaceuticals: Technical staff within Dental and Pharmaceutical Benefits Board supported by external experts136

Switzerland
  • Swiss Federal Office of Public Health (decisions)

  • Federal Drug Commission (recommendations)114,115

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals114

  • Patients and carers

  • Hospitals and hospital groups

  • Health care professional associations

  • Federal Office of Public Health114,137

  • Not specified

  • Manufacturer through submission requirements113

  • Federal Drug Commission114

The Netherlands
  • Ministry of Health, Welfare and Sport (decisions)

  • Medicinal Products Reimbursement Committee of the Dutch Healthcare Insurance Board (recommendations)116

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals31

  • University hospital federations, health care professional associations, and Dutch Healthcare Insurance Board for high-cost inpatient pharmaceuticals

  • Not specified

  • Manufacturer through submission requirements31

  • Technical staff within Dutch Healthcare Insurance Board117

  • Methods must comply with internationally recognize systematic review guidelines and Dutch Healthcare Insurance Board economic guidelines117

  • Technical staff within Dutch Healthcare Insurance Board117

United Kingdom
  • National Institute for Health and Clinical Excellence (decisions)

  • Technology Appraisals Committee (recommendations)7

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals

  • Patients and carers

  • Health care providers

  • Health care professional associations

  • General Public

  • National Horizon Scanning Centre120

Selection criteria:
  • Burden of disease (population affected, mortality, and morbidity)

  • Resource impact (on National Health Service costs and resources)

  • Clinical importance

  • Policy importance (alignment with government priority areas)

  • Inappropriate variations in practice

  • Likelihood of national guidance adding value7


Technology selection panel composition:
  • Health care providers (specialists, general practitioners, and public health professionals)

  • Patient representatives Technology selection panel makes recommendations. Final decisions made by Department of Health7

Single technology appraisals
  • Manufacturer through submission requirements120

Multiple technology appraisals
  • Independent academic group120

  • Methods must comply with National Institute for Health and Clinical Excellence systematic review and economic guidelines120

Single technology appraisals
  • Independent academic group120

Multiple technology appraisals
  • Independent academic group120

Wales
  • Ministry for Health and Social Services (decisions)

  • All Wales Medicines Strategy Group (recommendations)28

Referred by:
  • Manufacturers seeking reimbursement for newly approved pharmaceuticals28

  • Welsh Medicines Partnership horizon scanning process for identifying pharmaceuticals expected to receive market approval within 18 months28

  • Typically considered in order received28

  • Manufacturer through submission requirements28

  • Welsh Medicines Partnership28

  • Methods must comply with All Wales Medicines Strategy Group systematic review and economic guidelines28

  • Welsh Medicines Partnership28