指导
网站地图
英国作业 美国作业 加拿大作业
返回首页

research paper Sample

论文价格: 免费 时间:2010-09-18 15:38:03 来源:www.ukassignment.org 作者:留学作业网

research paper Sample

D:\research paper

Applying operations management logic and tools to save lives: A case study of the world health organization’s global drug facility

Abstract
In the field of operations management, theory concerning lead-time reduction is well developed. The application of lead-time reduction theory to the not-for-profit operations context, however, has been limited.We present an illustrative case study of a notfor profit operation in which long lead times cause a substantial increase in unnecessary deaths from tuberculosis and hinder the efforts of the World Health Organization to eradicate tuberculosis globally. The case study suggests that lead-time reduction theory may be as effective in not-for-profit (service) operations as it has been in manufacturing operations. Our results also illustrate how use of sophisticated but ‘‘user-friendly’’ queuing theory-based modeling tools can facilitate the acceptance and transfer of operations logic to a not-for-profit intergovernmental organization setting.

Keywords: Tuberculosis; Operations management; Lead-time reduction

1. Introduction
The purpose of this case study is to provide a brief illustrative example of the benefits of
transferring operations management logic and tools to a not-for-profit intergovernmental organization,
the Global Drug Facility (GDF) of the World Health Organization. As such, it is intended neither to
provide a comprehensive literature review of queuing theory applications in not-for-profit organizations
nor to extend theory concerning mathematicalmodeling of such operations. Rather, it provides an overview of how equipping doctors and
international civil servants with basic principles of operations management and then training them to
build simple queuing theory-based models of their process yielded lead-time reduction results that
could save lives. In addition to demonstrating the clear-cut applicability of a queuing model to an
intergovernmental organization, the more important contribution of this case study may well be to
illustrate the benefits of combining the transfer of straightforward operations management approaches
with simple modeling as a means for achieving buyin and implementation in the not-for-profit context,
where managers are not accustomed to thinking of themselves as running operations, and where the
emphasis on efficiency and cost reduction makes lead-time reduction even more difficult than in the
competitive arena faced by for-profit organizations.
The paper is organized as follows: Section 2 provides some brief background concerning TB and
the problems caused by long lead times in the intergovernmental operations working toward the
control and eradication of TB. In Section 3, we present our basic process analysis of the GDF
application processing operations, followed by a discussion of the queuing theory-based model developed
by the team. Results are presented in Section 4. In Section 5 we suggest implications of the study for#p#分页标题#e#
both the WHO and not-for-profit organizations.
2. A life-saving need for lead-time reduction It is now commonly agreed that TB control and
eventual elimination have shifted from being technical problems to being managerial and political challenges.
The tragedy of TB is that almost 2,000,000 people die annually (i.e., one person every 15 s) of a disease that
can usually be cured in 6months with $10worth of antituberculosis drugs (ATDs, Stop TB website, 2003).
Several decades ago, controlling TB was a top priority worldwide. The discovery of effective ATDs
led to a substantial reduction in TB in most developed countries; hence, TB control became a relatively low
priority. The same decline in TB cases did not occur in less-developed countries, however: By the late 1980s,
it became clear that TB was an urgent problem, especially when combined with the problems of
interaction with HIV infection and increasing outbreaks of multiple-drug-resistant strains of TB. Today,
8.5 million people develop TB every year, with 80% of these cases occurring in 22 ‘‘high burden’’ countries
(WHO, 2003). The WHO and other partner organizations responded to this crisis by forming the Stop TB
Partnership to mount a global attack on TB, setting global targets of detecting 70% of people with
infectious TB and curing 85% of those detected by the year 2005 (Raviglione and Pio, 2002).
The internationally recommended primary strategy for controlling TB is known as DOTS (which
originally stood for ‘‘directly observed treatment, short course’’). Between 1990 and 2001, the number
of countries that had an appropriate system for tuberculosis control rose from less than 10 to 155
(WHO, 2003) due to implementation of the DOTS strategy. It is generally agreed that the DOTS strategy
is the most effective strategy for controlling TB. The World Bank referred to DOTS as ‘‘one of the most cost
effective strategies available’’ (Stop TB website,2003). Dr. Gro Harlem Brundtland, then Director-
General of the WHO, referred to DOTS: ‘‘We have a cure. We need to mobilize the world to use it’’ (Stop
TB website, 2003).
In spite of the effectiveness of the DOTS strategy, however, the WHO estimated that in 2000, only 27%
of new cases were identified, implying that global targets for TB control would not be reached until the
year 2013 at the earliest (WHO, 2002). The major challenge in controlling TB is to ensure that patients
take their medication daily during the 6 months required for treatment. Efforts to ensure compliance
with treatment have been hindered, however, by lack of access to low cost ATDs of consistent quality. For
this reason, the Stop TB partners formed the GDF in early 2001 to fund and manage procurement and
quality assurance for countries applying for assistance.#p#分页标题#e#
The vision of the GDF is a TB-free world. Its mission is to: (a) ensure uninterrupted access to
quality TB drugs for DOTS implementation; (b) catalyze rapid DOTS expansion in order to achieve
global TB targets; (c) stimulate political and popular support in countries worldwide for public funding of
TB drug supplies; and (d) secure sustainable global TB control and eventual elimination (Global Drug Facility
website, 2003).
The GDF began their work with the objective that lead times from arrival of an application to delivery of
drugs to the port of the applying country would be less than 6 months (i.e., 132 working days); lead timeswould be reduced to 3 months (66 working days)
thereafter. However, in the first six countries supplied, the actual lead times averaged 267 working days, and
the average lead time has since increased to about 400 days (181 days for processing of applications – of
which about 20 days represent actual processing time – and 219 days from placement of order for drugs to
receipt of drugs in the applicant country). GDF management was uncertain regarding how to meet
lead time targets: It was generally agreed within the Stop TB organization that the GDF staff members
were working hard and displaying a high level of motivation.
A chance discussion brought lead-time reduction theory to the attention of the GDF manager, who then
invited a professor from the Operations Management department of a local university to work with his
group to explore the implications of applying existing theory concerning lead-time reduction to GDF
operations. We formed a team composed of the professor, the GDF manager, and an assistant from the
university who became employed by the GDF to work on the project. The objective of the GDF lead time
project was to explore the application of lead-time reduction theory in a not-for-profit organization to a
set of activities thatwould not normally be considered as an ‘‘operation.’’
3. Applying OM tools to the GDF operations Reviewing the mathematics of lead time and
carrying out a basic process analysis initiated the lead-time reduction efforts. However, a straightforward
mathematical tool was required to allow the group to reach consensus on courses of action,
communicate the action plan to the rest of the Stop TB unit so as to receive necessary approval and
funding, and transfer the vision for lead-time reduction to other operations within the WHO.
3.1. Initial analysis of GDF operations Following the principles of action research, the
project team examined the phenomenon of long lead times while working to create an action plan to reduce
the lead times. Action research, according to Greenwood and Levin (1998, p. 75), is ‘‘committed to the
idea that the test of any theory is its capacity to resolve problems in real life situations.’’ Another objective of#p#分页标题#e#
action research is practitioner learning, which results in an increase in the ability of practitioners to solve
problems.
A key aspect of the project entailed training the GDF staff both in the mathematical principles that
drive lead times and in building and interpreting queuing theory-based mathematical models of the
GDF operations, consistent with the objective of action research that practitioners become more able to
resolve their own problems through learning how to apply theory. Applying operations management theory
to a real problem also permitted testing and refinement of the theory in the context of an office operation in a
not-for-profit organization (see Rynes et al., 2001).
As mentioned previously, the actual processing time for applications was about 20 days, indicating
that 161 of the 181 days of lead time represented waiting time. Our objective was to use OM tools to
discover and make a plan for the elimination of this waiting.
We began by reviewing the relationships between bottleneck utilization, batch (lot) sizes, and lead time
(shown in Figs. 1 and 2). These relationships – fundamental to OM theory – were completely unfamiliar to the group. As soon as group members
understood these relationships, they immediately began to identify assumptions and behaviors that
had led to increased lead times. The GDF manager and S. de Treville et al. / Journal of Operations Management 24 (2006) 397–406 399
Fig. 1. As bottleneck utilization increases, average lead time increases at an increasing rate, becoming infinite at 100% utilization.his supervisor (the executive secretary of the Stop TB Partnership) were identified as primary bottlenecks,
but it was recognized that utilizations were also relatively high for other members of the team,
especially the two technical officers responsible for application processing.
Although it was initially assumed by the GDF manager that the relationship between batching and
lead times did not apply to GDF operations, it was subsequently determined that applications were
batched for review by a Technical Review Committee (TRC) that met three times per year. Stop TB
management had decided to hold the meetings every 4 months given the costs associated with bringing
together a large group of experts and because of the belief that all the experts should be together to make an
optimal decision concerning the applications. This www.ukassignment.org  meeting frequency implied that the ‘‘batch size’’ for
applications represented approximately 4 months’demand, which, according to the relationship shown
in Fig. 2, led to a substantial increase in lead times.
Development of a process flow diagram based on historical GDF records (shown in Fig. 3) and review of
the conceptual relationships between bottleneck utilization, batch sizes, and lead times helped the#p#分页标题#e#
group to understand some of the factors causing the long lead times. Our initial expectation was that we
would be able to explain the long waiting times using simple process analysis and commonsense reasoning.
We discovered, however, that we were able to account for only a portion of the 161 day waiting time using these tools due to the complexity of the process.
Quantifying the waiting time caused by high personnel utilization was complicated, for example, by the
substantial overtime worked by GDF personnel, combined with the fact that team members worked
half-time or less on application processing, with the rest of the time taken up by meetings or projects not
related to the processing of applications.
The team then attempted to determine how much of the 161-day waiting time could be explained by the
TRC-related batching of applications. Given that the TRC met three times per year, the team’s analysis
indicated an average increase in lead times of 2 months, or 44 working days (given 22 working days
per month) for applications requiring only a single TRC round. Applications, however, made on average
about 1.4 visits to the TRC1, which was expected to add another 35 days (40% of 88 working days), for a
total lead time impact of about 79 days. Commonsense reasoning, hence, suggested that approximately
half of the waiting time was due to this TRC-related batching.
Moving from this initial analysis to development of an action plan proved difficult. First, although the
GDF management was impressed by the impact of the TRC meetings on lead times, it was clear that the GDF
and Stop TB organizations were not prepared to take action to change the structure of the TRC meetings
based on this rather ad hoc analysis. The group’s initial reaction was that the frequency of the TRC meeting
could not be increased because TRC members were high-level officials of governments and other agencies
who were working pro bono: It would not be possible to ask them to come to the WHO headquarters in
Geneva, Switzerland, more frequently than three times per year. Furthermore, clearing applications through
the TRC was considered to be important in ensuring due diligence.
Similarly, the difficulties in quantifying the impact of high personnel utilization on waiting time made it
difficult to move acquisition of additional resources 400 S. de Treville et al. / Journal of Operations Management 24 (2006) 397–406
Fig. 2. Lead time increases approximately linearly with lot size.
Very small lots, however, may result in long lead times if setups cause high capacity utilization.
1 Some applications made two or more visits to the TRC. In estimating the average number of visits, we used the percentage of
applications sent back to the TRC on each round, which from Fig. 3 can be seen to be .07 + .71  .3 = .283. The percentage of applications
sent back n times we estimated as .283n. Summing as n goes from 0 to infinity yields an estimated number of visits of 1/#p#分页标题#e#
(1  .283) = .395.from a hope to a goal. Intergovernmental organizations such as the WHO operate under intense pressure
to increase resource utilization. Getting WHO and Stop TB management to change from efforts to
maximize resource utilization to being willing to add extra capacity (decreasing resource utilization) to
reduce lead times was going to take more than a cursory understanding of the relationships portrayed
in Figs. 1 and 2.
Finally, moving from theory to practice was hindered by the creativity generated by exposure to
OM concepts. The team had difficulty in knowing how to evaluate and prioritize the large volume of ideas that
arose from applying operations management theory.
For these reasons, we decided to build a mathematical model of the application processing operations to aid
in managing and evaluating the ideas generated, as well as to allow a more thorough analysis of the
process than was permitted by manual process analysis and commonsense reasoning. Application
processing was chosen as a starting point because the key parameters were under the control of the GDF.We
chose to use modeling software based on queuing theory rather than simulation because of its ease of
use. After this project, GDF team members should be able to construct and interpret queuing theory-based
models of processes, but it is unlikely that they would have been able to master simulation-based modeling
without extensive training. The software package used for the modeling was MPX (see Network Dynamics
website, 2003).
3.2. Building the queuing model
The model building began from development of the process flow diagram shown in Fig. 3. Processing
times were compiled by having a researcher work on site to interview and observe each member of the GDF
involved in processing applications. As processing times did not appear to demonstrate high variability,
we assumed a coefficient of variation of processing times of .3 (low variability according to Hopp and
Spearman, 1996, and the default value in the modelbuilding software).
As demonstrated in Fig. 3, the first step in the approval process was the screening of applications.
About 70% of applications had to be returned to the applicant for further information. Once the application
was judged complete, the information from the application was collected into a summary sheet and
submitted to the TRC. The decisions made by the TRC were summarized into notifications by the technical
officers. These notifications were approved by the executive secretary of the Stop TB Partnership (who
had supervisory responsibility for the GDF). TRC decisions resulted in an average of 7% of applications
being judged incomplete, requiring additional information from the applicant countries and an additional
TRC round 4 months later.
Country visits were required for the first grant awarded to each country. Once the TRC judged an#p#分页标题#e#
application coming from a first-time country complete, a country visit was planned by the technical
officers, approved by the Stop TB executive secretary, and carried out by technical officers, the GDF
manager, or a consultant appointed to the GDF.
Country visits were arranged for approximately 71% of applications evaluated by the TRC. Applications
judged complete from countries that already had been visited in connection with a previous application
(approximately 22% of applications evaluated by the TRC) proceeded directly to calculation of drug needs.
After the country visit, the GDF staff member prepared a report. In 30% of cases, the report indicated
a need for additional information and an additional round at the TRC. Once the country visit report
indicated that the file was complete, drug needs were calculated. Finally, the grant was prepared and the
application entered the drug-sourcing process.
Following the development of the process flow diagram, the next challenge was to set the lot sizes and
batching policies. Given that the TRC met three times per year, our initial inclination was to set the lot size at
one-third of the twenty applications processed each year. It was, however, necessary to increase the lot
sizes to reflect the 1.40 TRC rounds made by an average application; hence, we used an average lot
size of 20/3  1.40 = 9.3 applications.
The MPX software allows the user to set a transfer batch size that is different from the production lot size,
indicating that parts in a given batch are assumed to move to the next operation without waiting for the full
batch to be completed at that operation.2 A production 402 S. de Treville et al. / Journal of Operations Management 24 (2006) 397–406
2 Our terminology here matches that in the software: lot size for production, batch size for transfer.lot size of ten units combined with a transfer batch of
one unit would imply that the lot of ten pieces arrives together at the first workstation, with each piece
moving to the next workstation as soon as it is processed, with the ten pieces reassembled into the
original lot of ten after processing at the last workstation. The team compared this MPX logic to
the GDF application process.
In the GDF application process, applications tended to arrive just before the TRC meetings. There
was no intentional batching, but the TRC deadlines caused applications to be batched rather than arrive
uniformly throughout the year. Applications entered the TRC meeting as a batch: In fact, we modeled the
TRC meeting as a ‘‘setup time’’ because the time during which the meeting took place (5 days) was independent of the number of applications. The batch
of applications left the TRC meeting together and tended to be batched at several of the operations
following the TRC meeting. As an example, the executive secretary responsible for approving notifications#p#分页标题#e#
and country visits usually waited to process applications until he had the entire batch on his desk.3
The data used to construct the base case of the model are given in Tables 1 and 2.
4. Results
The application of the model yielded several potential improvements that could reduce the drug
approval process lead time from more than 180, to less than 40, working days. According to the base
case of the queuing model, lead times for processing applications averaged 183 days, compared to the
actual lead time of 181 days. The model highlighted three main causes of long lead times: ‘‘batching’’ of
applications, utilization levels for the technical officers handling applications, and the fact that
applications made an average of 1.4 visits through the TRC process. Using the model, we were able to
demonstrate that batching caused by the 4-month gap between meetings (‘‘time waiting for rest of lot’’)
was the primary cause of long lead times in processing applications, accounting for approximately
113 of the 183 days of lead time predicted by the model. Waiting for labor (i.e., an application
has arrived and is ready to be processed as soon as the relevant person arrives) accounted for 43 days of
lead times. The 5-day TRC meeting itself caused an average of 7 days lead time, given the 1.4 TRC
rounds required for an average application. Finally, run time (i.e., the time during which the application
was actually being processed) accounted for about 20 days, as expected.
Lead times predicted by the model are given in Table 3.We tested six scenarios in addition to the base
case:
In the first scenario, we added a technical officer on the demand side, which reduced the time waiting for
labor from 43 to 32 days and also reduced the time waiting for the rest of the lot by 6 days. The total
impact of adding a technical officer on the demand side was a reduction of about 17 days.
In the second scenario, we evaluated the impact of reducing the average number of TRC rounds per
application. As can be seen from Fig. 3, applications were returned to the applicant countries at two points
in the process: immediately after the TRC meeting (7%) and after the country visit (30%). These returns
were due to incomplete information, implying that the S. de Treville et al. / Journal of Operations Management 24 (2006) 397–406 403

Table 1
Model data (MPX format)
Time units
Operations Hours
Flow time Days
Production period Year
Hours per day 8
Days per year 210
Labor
Overtime (%) Unavailable (%)
1 Applicant 0 0
1 Consultant 0 0
1 Manager, GDF 50 55
1 Executive secretary, STB 0 70
2 Technical officers, demand 15 50
1 Technical officer, supply 15 50
Equipment for all employees modeled as having unlimited capacity  Demand/year Lot size#p#分页标题#e#
Product
Approved application 20 9.3
3 The instinctive tendency of people throughout the organization to batch applications supports our claim that instruction in lead time
reduction principles should not be limited to those officially working in operations.

frequencies could be reduced substantially through improved process documentation and support to the
applicant countries. To give GDF management an idea of the lead time implications of these repeat visits, we
modeled a scenario in which the percentage of applications returning to the TRC after the country
visit was reduced from 30% to 10%. This reduced the average number of TRC visits from 1.40 to 1.16,
implying a simultaneous reduction of the lot size from 9.3 to 7.7 to reflect the reduced number of repeat visits.
This scenario resulted in a 10-day reduction in waiting for labor because of the reduced processing required for applications, a 1-day reduction in average time spent at the TRC meeting (‘‘setup time’’), and a 23- day reduction in time waiting for the rest of lot. Run
time was reduced by 2 days because of the reduced
‘‘rework.’’ The overall lead-time reduction in this scenario was from 183 to 147 days.
404 S. de Treville et al. / Journal of Operations Management 24 (2006) 397–406
Table 2
Operation assignments and durations for application processing Operation Done by ‘‘Setup time’’
(h)
‘‘Run time’’ (h)
Application screening Technical officers, application side (TODs)
2
Request more information (after screening, TRC evaluation, or country visit) TODs 1.5
Information received from applicant
country after screening
Applicant country 56 (80%) 80 (20%)
Preparation of summary TODs 2
TRC evaluation TRC (including TODs) 40
Prepare notification TODs 1
Notification approval Executive secretary, Stop TB Partnership 0.5
Organize country visit TODs 16
Approval of country visit Executive secretary, Stop TB Partnership 1
Country visit TODs (25%), Technical officer, procurement (25%),
GDF manager (35%), Consultant (15%)
40
Preparation of country visit report TODs (25%), Technical officer, procurement (25%),
GDF manager (35%), Consultant (15%)
16
Calculation of drug needs TODs 2
Preparation of grant TODs 1
Clearance of grant Executive secretary, Stop TB Partnership 1
Grant acknowledgment Applicant country 24 (80%) 40 (20%)
Confirm grant TODs 1
Table 3
Impact of the different scenarios testedCombining the above two actions, we modeled
a scenario in which an extra technical officer was
added on the demand side and repeat visits to the TRC
after the country visit were reduced from 30% to 10%
of applications. http://www.ukassignment.org/liuxuezuoyedaixie/#p#分页标题#e#In this scenario, lead times were
reduced to 135 days, representing a 30-day improvement
compared to only adding a technical officer, and
a 12-day improvement compared to reducing the
repeat visits to the TRC without the addition of the
technical officer.
The next scenario considered a more extensive process redesign, in which the TRC was reconfigured to meet ‘‘virtually’’ to process each application, with
each virtual meeting taking 16 h of technical officer time. Under this scenario, the lead times for application processing dropped from 183 to about 64 days, that is, a reduction of 119 days. Run time was predicted to increase to 22 days, as the TRC evaluation was now modeled as a per unit processing time rather than as a setup time for a batch of applications.
Waiting for labor was predicted to decline slightly from the base case, dropping from 43 to 41 days. The 113 days of time spent waiting for the rest of the lot and the 7 days spent in the TRC meeting were eliminated.
Adding an extra technical officer to the virtual TRC meeting scenario reduced lead times still farther, to 45
days. Finally, combining virtual TRC meetings, an  xtra technical officer, and reduced repeat TRC visits
resulted in a lead time of 39 working days.
The team was surprised by how much was learned from the modeling exercise. Our initial expectation
was that modeling would provide limited value over manual process analysis. Not only were we able to quantify the impact of rework and high utilizations
easily, but also the impact of the TRC batching was far beyond the 79 days of waiting time that we had expected. Our commonsense reasoning substantially
underestimated the amount of waiting time caused by the applications exiting the TRC meeting as a batch. It
was only in interpreting the model results that we realized the extent of the batching-related waiting that
occurred at operations such as preparation and approval of country visits. Finally, the modeling
allowed us to capture the interaction effects between scenarios. We found it much simpler to discuss,
evaluate, and communicate action plans. What is more, the level of confidence in the team in OM
analysis increased tremendously once we could explain exactly why lead times were so long.
5. Implications for the WHO and other not-forprofit organizations
The next step in the project was to present the model to the entire Stop TB department to illustrate
the potential for lead-time reduction. In presenting the model, we explained that achieving model results
consistent with observed lead times required the addition of 15% overtime for the technical officers and
50% overtime for the director of the GDF, which we then observed to be consistent with practice. A minor –
but most appreciated – outcome of the modeling exercise was the opportunity it provided for Stop TB
and GDF management to explicitly acknowledge the  regular overtime worked by GDF staff members.#p#分页标题#e#
Based on the model results, Stop TB management made the decisions to: (a) add a technical officer,
especially since the workload of the technical officers was expected to increase over time; (b) formulate a
plan to increase the frequency of Technical Review Committee meetings—eventually to virtual meetings;
and (c) increase commitment to reduce process variability through standardization and documentation,
including a decision to seek ISO 9000 series certification. Based on these changes, the lead time for
application processing is in the process of being reduced from 6 months to the target of less than 2
months.
The doctors and global health care specialists involved in this project were unaccustomed to
considering themselves as ‘‘operations managers. Consistent with Suri’s (1994; 1998) empirical results,
these managers were unaware of the mathematical principles that drive lead times and were therefore
taking actions and making decisions that increased lead times. It was essential during the project to keep
the message and the underlying OM logic as simple and straightforward as possible to ensure maximum
buy-in and impact. When these doctors and speciali sts understood the mathematics of lead time, their
behavior began to change.
We expect that similar behavioral changes would result from this transfer of knowledge in other not-forprofit
organizations. To the extent that our results S. de Treville et al. / Journal of Operations Management 24 (2006) 397–406 405 generalize to other not-for-profit organizations, it may be worthwhile exploring ways to transfer knowledge concerning these OMand basic modeling principles to
all managers, whether or not they intend to ‘‘manage operations.’’ Finally, the positive response of these
doctors and specialists – as well as other doctors who saw the results – to mathematical modeling of
operations indicates a need for research into expanding the use of easily accessible modeling software
packages such as MPX.http://www.ukassignment.org/liuxuezuoyedaixie/
In the for-profit arena, access to the knowledge and tools required for managing lead times can easily
determine who wins and who loses competitively, with market share, profit, and investments in capacity and
inventory at stake. In organizations such as the GDF, however, such knowledge and tools translate into lives
saved. How many of those people currently dying needlessly of TB every 15 s will stay alive given
timely access to ATDs?

Acknowledgements
The authors would like to gratefully acknowledge the insightful comments of Bob Hayes, Roger Schmenner, Greg Diehl, and Guest Editor Bill Youngdahl.

References
Global Drug Facility website, 2003. Accessed December 21, 2003 from http://www.stoptb.org/GDF/whatis/whatis.html#p#分页标题#e#.
Greenwood, D.J., Levin, M., 1998. Introduction to Action Research:
Social Research for Social Change. Sage, Thousand Oaks, CA.
Hopp, W.J., Spearman, M.L., 1996. Factory Physics, first ed. Irwin
McGraw-Hill, Boston.
Network Dynamics website, 2003. Accessed March 6, 2003 from
http://www.networkdyn.com/RPMframe.html.
Raviglione, M.C., Pio, A., 2002. Evolution of WHO policies for
tuberculosis control, 1948–2001. The Lancet 359, 775–
780.
Rynes, S.L., Bartunek, J.M., Daft, R.L., 2001. Across the great
divide: Knowledge creation and transfer between practitioners
and academics. Academy of Management Journal 44 (2), 340–355.
Stop TB website, 2003. Accessed December 21 from http://
www.stoptb.org/tuberculosis/default.asp.
Suri, R., 1994. Common misconceptions and blunders in
implementing quick response manufacturing. In: Proceedings
of the SME AUTOFACT ’94 Conference, Detroit, MI,November.
Suri, R., 1998. Quick Response Manufacturing. Productivity Press,
Portland, OR.
World Health Organization, 2002. Global Tuberculosis Control:
Surveillance, Planning, Financing. WHO Report 2002. Geneva,
Switzerland, WHO/CDS/TB/2002.295.
World Health Organization, 2003. Global Tuberculosis Control:
Surveillance, Planning, Financing. WHO Report 2003. Geneva,
Switzerland, WHO/CDS/TB/2003.295.
 

此论文免费


如果您有论文代写需求,可以通过下面的方式联系我们
点击联系客服
如果发起不了聊天 请直接添加QQ 923678151
923678151
推荐内容
  • 历史Essay要求:Hist...

    ​本文是历史专业的Essay范例,题目是“HistoricalInvestigationofCanada’sFailureattheBattleofDieppe......

  • 社会学Essay格式:Sui...

    ​本文是社会学专业的留学生Essay范例,题目是“SuicideinNorthernCanada:ASociologicalPerspective(加拿大北部的......

  • 文化研究Essay范文:Ca...

    本文是文化研究专业的留学生Essay范例,题目是“Canadaacceptsimmigrants(加拿大接受移民)”,加拿大接受来自世界各地的移民,其中最重要的......

  • 护理学Essay参考案例:A...

    本文是护理学专业的留学生Essay范例,题目是“AnalysisofSickleCellDisease(镰状细胞病分析)”,随着来自发展中国家的人把加拿大当成自......

  • 政治Essay写作:Pros...

    ​本文是教育专业的Essay范例,题目是“ProsandConsoftheQuebecSeparationIssue(魁北克分离问题的利与弊)”,魁北克的分离在......

  • 文化研究Essay范文:It...

    本文是文化研究专业的留学生Essay范例,题目是“ItalianImmigrationtoCanada(意大利人移民加拿大)”,加拿大的东南海岸是在1947年6......

923678151