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WHO Medicines Strategy - Countries at the Core - 2004 - 2007
(2004; 163 pages) View the PDF document
Table of Contents
View the documentReview process and acknowledgements
View the documentAcronyms
Open this folder and view contentsHighlights
Open this folder and view contentsMedicines and public health
Open this folder and view contentsComponents of the strategy
Open this folder and view contentsImplementing the strategy - countries at the core
View the documentMonitoring progress with the strategy - measuring against indicators at country level
View the documentReferences
View the documentEndnotes
 

Monitoring progress with the strategy - measuring against indicators at country level


Figure 31: Monitoring Progress

It is important to have a regular source of information on the pharmaceutical situation at the country, regional, and global level that can be used as a guide for governments and stakeholders. This information should link to strategies and priority activities implemented in countries.

In recent years, WHO has developed a number of tools to track progress on key indicators and essential components of country pharmaceutical situations. One of these tools is the questionnaire on the structures and processes of the country pharmaceutical situation (the Level I questionnaire), which includes indicators that are collected from all Member States every four years.

Level I indicators provide a method to rapidly assess the implementation of national medicines policies and their components. These indicators are evaluated through a questionnaire completed at the national level. These core indicators are used to assess existing structures and processes in a national pharmaceutical system such as legislation/regulations, quality control of pharmaceuticals, essential medicines list, medicines supply system, medicines financing, access to essential medicines, production, rational use of medicines, intellectual property rights protection, and marketing authorization.

Information from Level I indicators are now being used by WHO to monitor its priority areas of work and to analyse country, regional, and global performance in the pharmaceutical sector. Country progress indicators corresponding to target outcomes in the WHO Medicines Strategy were selected mostly from Level I indicators.

Country progress indicators were identified based on expected activity outcome and challenging issues relevant to WHO work on pharmaceuticals. However, the indicators are intended to measure the collective efforts of the government and other groups, agencies, and stakeholders involved in pharmaceuticals.

The results of the 2003 survey have been compared against targets for the WHO Medicines Strategy 2000-2003 and used as baseline data for the 2004-2007 Strategy. New targets for each indicator were then established for the conclusion of the new Strategy by 2007 (see summary table of Country Progress Indicators below).

Country Progress Indicators for Expected Outcomes of WHO Medicines Strategy 2004-2007

Expected Outcomes and Indicators WMS 2004 - 2007

1999

1999

2003

2003

2003

2007

 

# Reporting

%

Target

# Reporting

%

Target

EO 1.1 Medicines policies developed, updated and implemented taking into consideration health, development, and intersectoral policies to achieve maximum impact

Countries with an official national medicines policy document - new or updated within the last 10 years

67/152

44%

55%

62/123

50%

59%

Countries with a national medicines policy implementation plan - new or updated within the last 5 years

41/106

39%

43%

49/103

48%

61%

EO 1.2 Implementation of medicines policy regularly monitored and evaluated, providing data that can be used in adjusting policy and interventions to improve access to medicines

Countries having conducted a national assessment of their pharmaceutical situation in the last 4 years

na

na

na

47/90

52%

58%

EO 1.3 Public health aspects protected in the negotiation and implementation of international, regional and bilateral trade agreements through inter-country collaboration and legislative steps to safeguard access to essential medicines

Countries integrating TRIPS Agreement flexibilities into national legislation to protect public health

na

na

na

32/105

30%

45%

EO 1.4 Human resources capacity increased in the pharmaceutical sector through education and training programmes to develop capacity and to motivate and retain personnel in sufficient numbers within a clearly defined and organized structure

Countries that provide both basic and continuing education programmes for pharmacists

54/85

64%

na

34/110

31%

35%

EO 1.5 Promotion of innovation based on public health needs, especially for neglected diseases, through policies and actions creating a favourable environment for innovation of medically needed new medicines

Countries promoting research and development of new active substances

na

na

na

21/114

18%

22%

EO 1.6 Gender perspectives introduced in the implementation of medicines policies by identifying gender differences in access to and rational use of medicines and supporting women in their central role in health care

Countries providing free medicines for pregnant women at primary public health facilities

na

na

na

54/106

51%

60%

EO 1.7 Access to essential medicines recognized as a human right via advocacy and policy guidance to recognize and monitor access to essential medicines as part of the right to health

Countries that provide HIV/AIDS-related medicines free at primary public health facilities

na

na

na

60/104

58%

65%

EO 1.8 Ethical practices promoted and anti-corruption measures identified and implemented in the pharmaceutical sector, using the experience of successful programmes addressing aspects of corruption encountered in the pharmaceutical sector

Countries with medicines legislation requiring transparency, accountability and code of conduct for regulatory work

na

na

na

84/114

74%

80%

EO 2.1 TM/CAM integrated in national health care systems where appropriate by developing and implementing national TM/CAM policies and programmes

Countries with national TM policy

25

na

na

39/127*

31%*

37%

EO 2.2 Safety, efficacy and quality of TM/CAM enhanced through expanding the knowledge base on safety, efficacy and quality of TM/CAM and providing guidance on regulation and quality assurance standards

Countries regulating herbal medicines

48

na

na

82/127*

65%*

75%

EO 2.3 Availability and affordability of TM/CAM enhanced through measures aiming to protect and preserve TM knowledge and national resources for their sustainable use

Countries with a national inventory of medicinal plants as a means to provide intellectual property rights protection for traditional medical knowledge

na

na

na

9/39

23%

33%

EO 2.4 Rational use of TM/CAM by providers and consumers by promoting therapeutically sound use of appropriate TM/CAM

Countries with national research institute in the field of TM/CAM

19

na

na

56/127*

44%*

51%

EO 3.1 Access to essential medicines improved, including medicines for HIV/AIDS, malaria, TB, childhood illnesses, and noncommunicable diseases

Countries where less than 50% of the population has access to essential medicines

29/184

16%

14%

15/103

15%

14%

EO 3.2 Public funding of medicines increased through increased organizational capacity to implement sustainable drug financing strategies and systems

Countries with public spending on medicines below US$2 per person per year

38/103

37%

35%

24/80

30%

20%

EO 3.3 Development assistance increased for access to medicines, including the Global Fund

Percentage of key medicines available in public health facilities

na

na

na

221

772

na

EO 3.4 Medicines benefits promoted within social health insurance and prepayment schemes

Countries with public health insurance covering the cost of medicines

71/111

64%

70%

79/117

68%

73%

EO 3.5 Medicine pricing policies and price information promoted to improve affordability of essential medicines

Countries with a pricing policy for maximum retail mark-up in the private sector

na

na

na

36/75

48%

55%

EO 3.6 Competition and generic policies implemented along with guidelines for maximizing competition in procurement practices

Countries in which generic substitution is allowed in private pharmacies

83/135

61%

75%

99/132

75%

81%

EO 4.1 Supply systems assessed and successful strategies promoted to identify weaknesses in the supply systems and improve the performance and functioning of national medicines supply systems

Countries with public sector procurement limited to national essential medicines list

71/133

53%

60%

84/127

66%

74%

EO 4.2 Medicines supply management improved through training programmes and career development plans to increase capacity and reduce staff turnover

Countries providing continuing education to pharmacists and pharmacy aides/assistants

39/103

38%

na

31/111

28%

32%

EO 4.3 Local production assessed and strengthened, on the basis of policy guidance to create a favourable environment for government or international support to domestic production of selected essential medicines

Countries with local production capability

na

na

na

36/122

30%

na

EO 4.4 Procurement practices and purchasing efficiency improved through guidance on good procurement practices, medicines management information support, and work with countries to strengthen efficient procurement procedures

Countries with at least 75% of public sector procurement carried out by competitive tender

81/88

92%

95%

58/70

83%

87%

EO 4.5 Public-interest NGOs included in medicine supply strategies, in support of national medicine supply strategies to reach remote areas

Countries with NGOs involved in medicines supply

na

na

na

29/64

45%

na

EO 5.1 Pharmaceutical norms, standards and guidelines developed or updated to promote good practice in regulatory matters

Countries using the WHO Certification Scheme as part of the marketing authorization process

na

na

na

87/135

64%

75%

EO 5.2 Medicines nomenclature and classification efforts continued through assignment, promotion and protection of international nonproprietary names, and the promotion and development of ATC/DDD system.

Countries using INNs in medicines registration.

na

na

na

108/131

82%

90%

EO 5.3 Pharmaceutical specifications and reference materials developed and maintained for use in quality control laboratories and publications in the International Pharmacopoeia

Number and types of pharmaceutical specifications and reference materials developed by WHO HQ

na

na

105

96

na

50

EO 5.4 Achieving balance between abuse prevention and appropriate access to psychoactive substances through enhancing the implementation of relevant guidelines to promote rational use of controlled medicines

Number of substances reviewed and recommended for classification for international control

2/3.

66%

na

5/5.

100%

80%

EO 6.1 Medicines regulation effectively implemented and monitored as the capacity of staff is increased through training activities resulting in better knowledge, organization, financing, and management

Countries implementing basic medicines regulatory functions

70/138

51%

56%

90/130

69%

74%

EO 6.2 Information management and exchange systems promoted and made accessible through shared databases. Basic regulatory information made available to the general public

Countries with a computerized medicines registration system

na

na

na

72/135

53%

60%

EO 6.3 Good practices in medicine regulation and quality assurance systems to ensure that product quality is maintained in production, clinical trials, supply and distribution

Countries with basic quality assurance procedures

95/122

78%

80%

111/137

81%

85%

EO 6.4 Post-marketing surveillance of medicine safety maintained and strengthened through the ongoing development of pharmacovigilance centres and their involvement in international adverse drug reaction monitoring systems

Countries monitoring adverse drug reactions

56/191

29%

35%

72/192

38%

45%

EO 6.5 Use of substandard and counterfeit medicines reduced as a result of the development and application of effective strategies to detect the existence and combat the production and circulation of such products

Countries with >10% of tested medicines failing quality tests

na

na

na

20/71

28%

25%

EO 6.6 Prequalification (initial assessment, ongoing monitoring and prequalification) of products and manufacturers of medicines for priority diseases; and of quality control laboratories, as appropriate, through procedures and guidelines appropriate for this activity

Number of products assessed and approved

na

na

na

93

na

na

EO 6.7 Safety of new priority and neglected medicines enhanced through training workshops and increased capacity to assess safety issues

Countries participating in training programmes for introducing new therapies for priority and neglected diseases, e.g. malaria and AIDS

0

na

na

7

na

20

EO 6.8 Regulatory harmonization monitored and promoted as appropriate, and networking initiatives developed, to facilitate and improve regulatory processes in countries

Number of countries participating in harmonization initiatives supported financially and technically by WHO

na

na

na

15/191

8%

18%

EO 7.1 Rational use of medicines by health professionals and consumers advocated

Countries where the promotion of the rational use of medicines is coordinated at the national government level

na

na

na

93/127

73%

75%

EO 7.2 Essential medicines list, clinical guidelines and formulary process developed and promoted

Countries with national list of essential medicines updated within the last 5 years

129/175

74%

75%

82/114

72%

75%

Countries with treatment guidelines updated within the last 5 years

60/90

67%

70%

47/76

62%

65%

EO 7.3 Independent and reliable medicines information identified, disseminated and promoted

Countries with a national medicines information centre able to provide independent information on medicines to prescribers and/or dispensers

62/123

50%

59%

53/129

41%

50%

Countries with a medicines information centre/service accessible to consumers

na

na

na

45/127

35%

40%

EO 7.4 Responsible ethical medicines promotion for health professionals and consumers encouraged

Countries with basic system for regulating pharmaceutical promotion

92/132

70%

80%

83/113

73%

76%

EO 7.5 Consumer education enhanced in recognition of the growing significance of self-medication and of consumer access to knowledge and advice of variable quality

Countries that have implemented a national consumer education campaign in the last two years

na

na

na

72/120

60%

60%

EO 7.6 Drug and therapeutics committees promoted at institutional and district/national levels

Countries with DTCs in the majority of regions/provinces

na

na

na

32/96

33%

40%

EO 7.7 Training in good prescribing and dispensing practices promoted

Countries that include the concept of essential medicines in basic curricula for medicine and/or pharmacy

na

na

na

72/88

82%

85%

EO 7.8 Practical approaches to contain antimicrobial resistance developed based on the WHO Global Strategy to Contain Antimicrobial Resistance

Countries with national strategy to contain antimicrobial resistance

na

na

na

37/113

33%

40%

EO 7.9 Identification and promotion of cost-effective strategies to promote rational use of medicines

Countries that have undertaken a national assessment/study of the rational use of medicines

na

na

na

57/97

59%

60%

 

* Data collected from Traditional Medicine Survey

 

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Last updated: May 3, 2013