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Defect in the South African construction industryLe Roux, Martyn January 2012 (has links)
Lack of quality in the South African construction industry is causing various problems for different stakeholders. The causes of this lack in quality are due to various different attributes. Corruption has become one of the leading causes with regards to lack of quality. Quality assurance can mitigate or eliminate defects through the implementation of a quality management system. Defects manifest primarily through cracking, dampness, detachment, and water leaks. Defects are categorized as structural, subsidence, acoustic and thermal. In terms of time, defects are either patent or latent, and can be discovered through observation, inspection and various tests. The causes of defects are ultimately due to error or omission, either during design or during the construction phases. Defects may also result due to procurement related factors, such as appointment of incompetent contractors. The result of defects is customer dissatisfaction, rework and disputes. Non-conformance to requirements results in rework and this in turn contributes to time and cost overruns. The aim of this research was to investigate the greatest cause that leads to defects in houses; the most common type of defect; and why projects fail in term of project management terms (due to defects). Results of quantitative research amongst professionals within the construction industry in the Western and Eastern Cape of South Africa as well as literature that has been reviewed form the basis of this study. Architectural practices, consulting engineering practices, and general building contractors were selected on a random sample basis, and surveyed using an online questionnaire. The study revealed that inadequate artisan skills is the biggest cause leading to defects in houses, and that cracks are the most frequent type of defect occurring. Projects fail in project management terms because of defects as the construction time of the projects are increased. The study revealed that construction related causes of defects dominate over design related causes. This study should be of value to both construction industry professionals as well as their clients.
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The impact of quality assurance systems on the operational performance of laboratoriesRatsoeu, Ellen 30 May 2013 (has links)
M.Tech. (Operations Management) / It has become a trend for organisations to implement and certify quality systems. The most common quality system that organisations currently implement is ISO 9001. Certification to ISO 9001 has in recent times been used as a marketing tool to enter new markets. Nowadays, customers expect their suppliers and potential suppliers to be certified to ISO 9001. It has become a primary requirement for doing business, and customers now demand it. There have been various studies conducted to establish the advantages of ISO 9001 and its impact on organisational performance. Laboratories are no exception to this developing trend. They are implementing laboratory quality standards like ISO 17025 and the Organisation for Economic Cooperation and Development Good Laboratory Practice (OECD GLP). Some laboratories are now applying for certification of compliance to laboratory standards. Implementing and certifying laboratory systems is an exercise that comes at a cost. The exercise is demanding in terms of human resources, time and capital. There has not been a study conducted to evaluate the impact of these systems on the operational performance of laboratories. This is the reason that resulted in identification of the need to conduct the study. A qualitative research approach was pursued in conducting the study, where the researcher investigated the impact of laboratory quality standards on the operational performance of commercial and non-commercial laboratories. Operational performance in this study is defined as health and safety; supplier selection and performance; human resources; customer satisfaction and profitability. Data was collected through interviews, and was then summarised, and analysed in order to address the research problem. Based on the data collected, it was concluded there is no notable difference in the performance of laboratories with or without quality assurance systems such as ISO 17025 and OECD GLP.
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Impact of ISO 9000 certification on quality management practices among SMEs in the Western Cape, South AfricaDase, Bonginkosi January 2016 (has links)
Thesis (MTech (Quality))--Cape Peninsula University of Technology, 2016. / The study has been carried out on impact of implementing ISO standards on SMEs to seek general evaluation of its benefits. The purpose of this paper is to outline the benefits of ISO implementation on South African small- and medium-sized enterprises (SMEs). The SME sector is the backbone of developed economies, which is regarded as the engine of growth for economies all over the world. For developing countries, SMEs often offer the only realistic prospects for increases in employment since they employ the largest percentage of the workforce population. With the trend towards global market orientation and trade liberalisation, SMEs are moving towards implementing quality systems. The empirical study aims to explore current implementation of quality management tools and advanced improvement techniques in the Western Cape SMEs, in order to understand what factors impact on how quality control is managed.
Two main categories are analysed, namely tangible and intangible. This study will assist other SMEs in developing countries on ISO 9000 implementation. This study is restricted to small and medium-sized companies in South Africa implementing ISO system and other quality tools or techniques. Data collection of this study is done based on a combination of survey questionnaires and interviews with managers, supervisors and general staff.
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Development and validation of stabilized whole blood samples expressing T-cell activation markers as quality control reference materialLouw, Anne-Rika 03 1900 (has links)
Thesis (MScMed)--Stellenbosch University, 2008. / ENGLISH ABSTRACT: Introduction: Flow cytometry has progressively replaced many traditional laboratory
tests due to its greater accuracy, sensitivity and rapidity in the routine clinical settings
especially clinical trails. It is a powerful tool for the measuring of chemical (the
fluorochrome we add) and physical (size and complexity) characteristics of individual
cells. As these instruments became major diagnostic and prognostic tools, the need for
more advanced quality control, standardized procedures and proficiency testing
programs increased as these instrumentations and their methodology evolve. Minor
instrument settings can affect the reliability, reproducibility and sensitivity of the
cytometer and should be monitored and documented in order to ensure identical
conditions of measurement on a daily basis. This can be accomplished by following an
Internal Quality Assurance (IQA) and/ or External Quality Assurance (EQA) program.
Currently there are no such programs available in South Africa and poorer Africa
countries. HIV is a global concern and the laboratories and clinics in these places are in
need of such IQA programs to ensure quality of their instrumentation and accurate
patient results. Quality assurance programs such as CD Chex® and UK Nequas are
available but due to bad sample transport, leave the receiving laboratories with
nightmares. It would be best if there was a laboratory in South Africa that could
provide the surrounding laboratories with stabilized whole blood samples that can be
utilized as IQA. The transport of these samples can be more efficient due to shorter
distance and thus the temperature variations limited. Aims and Objectives: The aim of Chapter one is to familiarize the reader with general
terminology and concepts of immunology. Chapter two describes in detail the impact
stabilized whole blood had on clinical immunology concerning Quality Control and
Quality Assurance. The objective of this study is to stabilize whole blood with a shelf
life of greater than 30 days to serve as reference control material for South African
Immunophenotyping. It is further an objective to use these in-house stabilized control
samples for poorer African countries as Internal Quality Assurance reference material.
It is a still further objective to stimulate various lymphocyte subsets to express
activation antigens and then stabilize these cells for more specialized immunological
test and can serve as a QC for those required samples.
Study design: In Chapter three, the method currently used to stabilize whole blood was
modified. The stability of different concentrations of a first stabilizing agent
(Chromium Chloride hexahydrate) was investigated. Incubation periods and
concentrations of paraformaldehyde as second stabilizing agent were investigated.
Blood samples from healthy individuals (n=10) were stabilized and monitored for the
routine HIV phenotypic surface antigens over a period of 40 days. These samples
(n=10) were compared on the Becton Dickinson Biosciences (BD) FACSCalibur™
versus BD FACSCount™ instrumentation. Blood samples (n=3) were stabilized and
monitored to identify phenotypic cell surface molecules for as long as possible. They
were quantified on both flow cytrometric instruments. In addition, these stabilized
samples (n=3) were investigated as control blood for calibration purposes on the BD
FACSCount™ instrument. In Chapter four, lymphocytes were isolated and activated with various stimuli to
express sufficient activation antigens such as CD25, CD69, HLA-DR and CD40
Ligand on the T helper cell surfaces. These activated antigens were analyzed on the
BD FACSCalibur™ and further stabilized to serve as possible IQA samples in future.
Results: In Chapter three, the ten individual stabilized samples had non-significant P
values (P > 0.05) for CD3, CD4 and CD8 percentages and absolute values comparing
day 3 until day 40. Comparing the BD FACSCalibur™ versus BD FACSCount™,
resulted in a R2 = 0.9848 for CD4 absolute values and a R2 = 0.9636 for CD8 absolute
values. Stabilized blood samples (n=3) were monitored for routine HIV phenotypic
markers until day 84. The cells populations were easily identifiable and could be
quantified on both BD FACSCalibur™ and BD FACSCount™ instruments.
In Chapter four; for the activation study purposes, activated T helper lymphocytes
expressed approximately 25 to 35% CD40 Ligand cell surface molecules. The
stimulant of choice was Ionomycin at a 4μM concentration. Cells were incubated for
four hours at 37 degree Celsius in a 5% CO2 environment. For CD69 surface
expression, 6 hour incubation was optimum. The stimulus of choice in this case was
4μM Ionomycin which induced 84.21% CD69 expression in the test samples. For
CD25 expression; 6 hour incubation with PHA resulted in approximately 43% of CD25
expression. For HLA-DR surface expression; 6 hour incubation with PHA resulted in
approximately 43.32% of HLA-DR expression. Activated lymphocytes expressing
CD40 Ligand showed stability until day 23. Activated Lymphocytes expressing CD69,
CD25 and HLA-DR were stabilized in the same manner and stability could be
achieved until day 16. Conclusion: This thesis was related to the preparation of control samples (IQA)
designed to simulate whole blood having defined properties in clinical laboratory
situations. In future kits can be developed with a low, medium and high control sample
for the various immunological phenotypic determinants. Another kit can be compiled
where various activation markers can be identified, quantified with a “zero”, low and
high control. These whole blood IQA kits and “activation IQA kits” can be
implemented for training of newly qualified staff, competency testing of staff, method
development, software testing, panel settings and instrument setting testing. Control
samples ideally must have a number of properties in order to be effective. For instance
stability during storage times, preferably lasting more than a few weeks,
reproducibility and ease of handling. These will provide the information on day-to-day
variation of the technique or equipment which will enhance accuracy and improve
patient care. / AFRIKAANSE OPSOMMING: Inleiding: Vloeisitometrie tegnologie het verskeie tradisionele laboratorium toetse
vervang as gevolg van beter akuraadheid, sensitiwiteit en vinniger beskikbaarheid van
resultate in ‘n kliniese omgewing, veral kliniese proewe. Vloeisitometrie is ‘n kragtige
tegniek om chemiese (fluorokroom byvoeging) en fisiese (sel grote en kompleksiteit)
karakter eienskappe van individuele selle te meet. Met die toename in gebruik en
gewildheid van hiedie instrumente, neem die behoefde toe vir gevorderde kwaliteit
kontroles, gestandardiseerde prosedures, met profesionele toets programme tesame met
metode ontwikkeling.
Klein verstellings aan instrument parameters beinvloed die betroubaarheid,
herhaalbaarheid en sensitiwiteit van ‘n sitometer en moet gemonitor (en dokumenteer)
word om identiese kondisies van leesings op ‘n daaglikse basis te verseker. Dit kan
bereik word deur in te skakel met ‘n interne kwaliteits versekerings program [IQA:
“Internal Quality Control”] en/of ‘n eksterne kwaliteits versekerings program [EQA:
“External Quality Control”] te volg. Op die oomblik is daar geen sulke kwaliteits
versekerings programme in Suid Afrika en/of in die verarmende Afrika lande
beskikbaar nie. MIV is ‘n wêreldwye bekommernis en laboratoriums en klinieke in
hierdie gedeeltes van die land verlang ‘n dringende behoefdte vir sulke “IQA”
programme om kwaliteit van instrumentasie en akkurate pasiënt resultate te verseker
wat tot beter behandeling van pasiënte lei. Kwaliteit versekerings programme soos
“CD Chex®” en “UK Nequas” is beskikbaar, maar baie probleme met verwysing na
monster integriteit as gevolg van tydsame vervoer en aflewering kondisies word
hiermee geassosieër. Die behoefte het ontstaan vir ‘n laboratorium in Suid Afrika wat direk die omliggende
laboratoriums, hospitale en klinieke kan voorsien met gestabiliseerde blood monsters
wat gebruik kan word as “IQA”. Die vervoer en aflewerings kondisies van hierdie
monsters sal aansienlik verbeter as gevolg van die korter aflewerings afstand wat direk
die beperkte temperatuur wisseling beinvloed.
Doel van studie: Die doelwit van hoofstuk een is om vir die leser ‘n inleiding te gee
tot terminologie en konsepte van immunologie en die immune sisteem. Hoofstuk twee
beskyf die impak wat gestabiliseerde heelbloed het op die kliniese immunologie met
betrekking tot kwaliteit beheer en kwaliteit versekering. Die doelwit van hierdie studie
is om heelbloed te stabiliseer sodat die rakleeftyd meer as 30 dae is en sodoende as
verwysings-materiaal kontroles vir Suid Afrikaanse immunofenotipering kan dien. Dit
is ‘n verdere doelwit om hierdie tuis-gestabiliseerde kontrole monsters te gebruik as
“IQA” verwysings materiaal in verarmende Afrika lande. Die doelwit van hoofstuk
vier is om limfosiete te stimuleer om verskeie aktiverings merkers uit te druk op hul
selmembrane en dan te stabiliseer en dié te gebruik as Kwaliteits Kontroles vir die
meer gespesialiseerde immunologiese toetse.
Studie ontwerp: Hoofstuk drie beskryf ‘n aangepaste en verbeterde metode van heel
bloed stabiliseering. Stabiliteit word ondersoek in ‘n verskyndenheid konsentrasies van
‘n primêre stabiliseerings agent (chromium chloried heksahidraat) en inkubasie
periodes met paraformaldehied as tweede stabiliseerings agent word deeglik
gedokumenteer. Bloedmonsters van gesonde indiwidië (n=10) was gestabiliseer en
gemonitor vir roetine MIV membraanoppervlak antigene oor ‘n periode van 40 dae. Hierdie monsters (n=10) was gelees en geanaliseer op ‘n BD FACSCalibur™ en
vergelyk met ‘n BD FACSCount™ vloeisitometer instrument. Drie gestabiliseerde
heelbloed monsters (n=3) was gemonitor vir ‘n periode vir so lank moontlik die
fenotipiese selmembraan molekules identifiseerbaar was en die kwantiteit bepaalbaar
was. Hierdie drie monsters was gemeet op beide instrumente. As ‘n addisionele
doelwit, was hierdie drie gestabiliseerde monsters ondersoek om as moontlike
kalibrasie materiaal (verteenwoordig ‘n normale bloedmonster) te dien vir die BD
FACSCount™ instrument in die oggende voor pasiënt monsters gelees kan word.
In hoofstuk vier was limfosiete geϊsoleer en geaktiveer met ‘n verskyndenheid
stimulante om optimale aktiveerings-antigene uit te druk op T helper selmembrane
(byvoorbeeld CD25, CD69, HLA-DR en CD40 Ligand). Hierdie geaktiveerde
monsters was geanaliseer op die BD FACSCalibur™ en daarna gestabiliseer. Na
stabilisasie van die geaktiveerde limfosiet monsters was dit gemonitor oor ‘n tydperk
so lank moontlik data plotte leesbaar en selpopulasies identifiseerbaar was. Hierdie
monsters kan dien as ‘n moontlike “IQA” toets stel vir ‘n meer gespesialiseerde
immunologiese aktiveerings kontrole doeleindes.
Resultate: In hoofstuk drie; tien individiële gestabiliseerde heelbloed monsters het
gedui op geen-beduidende P waardes (P > 0.05) vir CD3, CD4 en CD8 persentasies en
absolute waardes; gemeet vanaf DAG 3 vergelykbaar tot-en-met DAG 40. Met korrelasie statistiek en vergelyking van die BD FACSCalibur™ met die
FACSCount™ instrumente, is die volgende opgemerk; R2 = 0.9848 vir die CD4
absolute waardes en ‘n R2 = 0.9636 vir die CD8 absolute waardes. Drie gestabiliseerde
monsters (n=3) was gemonitor vir MIV roetine fenotipeering tot en met DAG 84. Die
selpopulasies was duidelik identifiseerbaar en die kwantitatief meetbaar op albei
instrumente (BD FACSCalibur™ en BD FACSCount™).
Hoofstuk vier: geaktiveerde T helper lymphosiete het 25 – 35% membraan CD40
Ligand uitgedruk op hul selmembrane. Die stimulant van keuse was ionomysien teen
‘n optimale konsentrasie van 4μM. Die optimale inkubasie tydperk was vier ure by
37°C in 5% CO2 kondisie. Ses uur inkubasie in 4μM ionomysien by 37°C in ‘n 5%
CO2 omgewing was optimal vir die CD69 selmembraan uitdrukking en het 84.21%
opgelewer. Vir CD25 selmembraan uitdrukking was die selle vir ses ure met
phietoheamagglutinin (PHA) gestimuleer by 37°C in 5% CO2 kondisie en het 43%
CD25 selmembraan uitdrukking opgelewer. HLA-DR selmembraan uitdrukking: selle
was vir ses ure saam met PHA by 37°C in 5% CO2 kondisie inkubeer en het 43.32%
opgelewer. CD40 Ligand aktivering/gestabiliseerde limfosiete het tot en met dag 23
stabiliteit getoon. Die ligand was duidelik identifiseerbaar en kwantifiseerbaar.
Geaktiveerde lymphosiete wat CD69, CD25 en HLA-DR selmembraan merkers
uitdruk het na die stabiliseerings proses stabiliteit getoon tot-en-met dag 16. Gevolgtrekking: Die doel van hierdie studie was om verwysingskontroles voor te
berei sodat dit vars heelbloed naboots met uitkenbare eienskappe vir kliniese situasies.
‘n Toets kontrolestel met verwysings materiaal vir drie vlakke (byvoorbeeld ‘n lae,
medium en hoë kontrole) absolute selwaardes en persentasies kan voorberei word vir
roetine immunologiese fenotiperings merkers (CD3/CD4/CD8/CD45). Meer
gespesialiseerde kontrolestelle vir meer spesifieke doeleindes kan opgemaak word wat
‘n verskydenheid van limfosiet aktiveringsmerkers bevat met byvoorbeeld ‘n “nul”, lae
en hoë verwysings kontrole daarin. Hierdie heelbloed kan dien as “aktiveerde interne
kwaliteits verwysings materiaal” en kan gebruik word om nuut aangestelde
laboratorium werkers en nuut gekwalifiseerde studente op te lei. Hierdie verwysings
materiaal / kontroles kan aangewend word vir bevoegdheids doeleindes (byvoorbeeld
vir SANAS akkreditasie doeleindes), vir metode ontwikkeling, vir sagteware toetsing,
vir paneel opstelling en instrument verstellings doeleindes. Die kontroles moet ‘n
verskydenheid eienskappe bevat om effektief te wees. Byvoorbeeld, stabiliteit tydens
storing, gewenslik meer as ‘n paar weke, herhaalbaar en maklik handteerbaar. Hierdie
kontroles sal inligting voorsien op ‘n daaglikse basis tydens wisseling van tegnieke of
instrumentasie wat akuraatheid beinvloed en op die ou-end direk pasiënt versorging
bevoordeel.
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Onderwysers se ervaring van die doel en die implementering van Geïntegreerde Gehaltebestuurstelsel (GGBS)Sass, Jan Johannes 12 1900 (has links)
Thesis (MEd (Education Policy Studies))--University of Stellenbosch, 2010. / Bibliography / ENGLISH ABSTRACT: Evaluation is seen as one of the key elements to enhance the teaching skills and
subject knowledge of teachers, thereby facilitating effective and quality teaching and
learning. One way of ensuring that this becomes a reality at South African schools is
the introduction of an evaluation policy, namely the Integrated Quality Management
System, as contained in the document Integrated Quality Management System
(IQMS), Collective Agreement Number 8 of 2003 of the Education Labour Relations
Council. This research was conducted against the backdrop of IQMS implementation
in South African schools since 2005, and explored answers to the following
questions: How do teachers experience the implementation of the IQMS (a form of
evaluation)? To what extent does the IQMS contribute to the support, development
and growth of teachers? Has the implementation of the IQMS had any positive
impact on the quality of teaching and learning in schools?
The data for the research were collected in 39 schools in Paarl and surrounding
areas. The findings of the research study are based on a quantitative (questionnaire)
investigation in the framework of an interpretive and positivistic paradigm.
The results of the research showed that a significant number of teachers experience
the goal and implementation of the IQMS as problematic. This leads to the
conclusion that the implementation of the policy has not necessarily contributed to a
fundamental improvement in the quality of teaching and learning in the participating
schools. This conclusion is also based on the lack of meaningful and ongoing support
and assistance that respondents receive before and after the evaluation process.
The findings of this study correspond with those of international studies on the same
topic, and indicate that teachers face universal problems, particularly with regard to
the implementation of evaluation policies. This study could contribute to further
research on the topic. / AFRIKAANSE OPSOMMING: Evaluering word as een van die kernelemente beskou om onderwysers se
onderrigvaardighede en vakkennis te verbeter, en sodoende doeltreffende en goeie
onderrig en leer in die hand te werk. Een manier om toe te sien dat dít in Suid-
Afrikaanse skole werklikheid word, is die instelling van evalueringsbeleid, oftewel
die Geïntegreerde Gehaltebestuurstelsel (GGBS), soos dit in die dokument
Integrated Quality Management System (IQMS), Collective Agreement Number 8 of
2003 van die Raad op Arbeidsverhoudinge in die Onderwys vervat word. Hierdie
studie is teen die agtergrond van GGBS-inwerkingstelling in Suid-Afrikaanse skole
sedert 2005 onderneem, en soek na antwoorde op die volgende vrae: Hoe ervaar
onderwysers die inwerkingstelling van die GGBS ( vorm van evaluering)? In watter
mate dra die GGBS by tot die ondersteuning, ontwikkeling en groei van
onderwysers? Het die inwerkingstelling van die GGBS enige positiewe invloed op die
gehalte van onderrig en leer in skole?
Die data vir die navorsing is in 39 skole in die Paarl en omgewing ingesamel. Die
bevindings van die navorsingstudie is gegrond op kwantitatiewe (vraelys-)
ondersoek in vertolkende en positivistiese paradigma.
Die navorsingsresultate toon dat beduidende aantal onderwysers die doel en
inwerkingstelling van die GGBS as problematies ervaar. Dít lei tot die gevolgtrekking
dat die inwerkingstelling van die beleid nie noodwendig tot grondliggende
verbetering in die gehalte van onderrig en leer in die deelnemerskole gelei het nie.
Dié gevolgtrekking berus ook op die gebrek aan sinvolle en deurlopende
ondersteuning en hulp wat die respondente voor en ná die evalueringsproses
ontvang.
Die bevindings van hierdie studie stem ooreen met dié van internasionale studies oor
dieselfde onderwerp, en toon dat onderwysers, bepaald wat die inwerkingstelling van
evalueringsbeleid betref, met universele probleme te kampe het. Hierdie studie kan
tot verdere navorsing oor die onderwerp bydra.
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Organisational culture and external quality assuranceNaidoo, Dhanasagran 12 1900 (has links)
Thesis (PhD (Curriculum Studies))--University of Stellenbosch, 2009. / ENGLISH ABSTRACT: Organisational culture and external quality assurance in higher education have both
drawn significant attention to their promise of greater organisational effectiveness and
efficiency and enhanced, improved higher education respectively. In recent years, these
constructs have been linked by an assumption that an organisational culture that is
amenable to change would be more receptive to the introduction of formal external
quality‐assurance structures, systems and instruments, as these are aimed at effective
and efficient higher education practices, processes and outcomes. However, this
assumption has not been sufficiently tested given that there are significant philosophical,
conceptual and methodological controversies and contestations surrounding both
constructs. While the organisational culture literature has been littered with a
proliferation of paradigms and, albeit, fragmented theories, there has been a paucity of
theory building in the corresponding literature on quality in higher education in general
and on the impact of external quality assurance on institutions specifically.
A qualitative case study was conducted at a newly merged university of technology to
investigate two taken‐for‐granted assumptions: first, that organisational cultures are
homogenous, unitary and centred around shared values and could therefore easily be
manipulated (usually from the top by management), and second, that the introduction of
external quality assurance is an unproblematic technology that will be accepted without
question by higher education institutions as it was premised upon the laudable aim of
improving the quality of those institutions. A conceptual four‐perspective framework was
developed to critically evaluate the literature and provide the basis for the threedimensional
model used in analysing the findings. The research generated several key
conclusions that appear to challenge commonly held and articulated positions with
regard to organisational culture and external quality assurance. First, organisational
culture should be considered as being more ephemeral than concrete, multidimensional
than singular, characterised simultaneously by conflict, consensus and indifference and in
a constant state of flux. Second, external quality assurance is not necessarily a value‐free
and neutral exercise aimed at improving the quality of teaching and learning, as promised
in its early conceptualisation and implementation. Third, multiple cultures may exist
simultaneously, interact with and influence each other constantly and of course
determine interactions within the organisation and the nature of engagement with
externally originated initiatives. Fourth, external quality assurance has purposes that go
beyond its often morally just and public‐good motives as it tacitly and overtly acts as an
agent of control, empowerment and transformation and simultaneously as an agent of
the state, though not necessarily to the same extent. / AFRIKAANSE OPSOMMING: Organisatoriese kultuur en eksterne gehalteversekering in hoër onderwys het albei die
aandag in groot mate gevestig op hulle belofte van groter organisatoriese
doeltreffendheid en doelmatigheid en gevorderde, verbeterde hoër onderwys
onderskeidelik. In die afgelope paar jaar is hierdie konstrukte byeengebring deur ʼn
veronderstelling dat ʼn organisatoriese kultuur wat vatbaar is vir verandering, meer
ontvanklik sal wees vir die invoer van formele eksterne strukture, stelsels en instrumente
vir gehalteversekering, aangesien dit op doeltreffende en doelmatige praktyke, prosesse
en uitkomste vir en van hoër onderwys gerig is. Hierdie aanname is egter nie voldoende
getoets nie gegee die feit dat daar aansienlike filosofiese, konseptuele en metodologiese
strydvrae en twispunte ten opsigte van albei konstrukte bestaan. Terwyl literatuur oor
organisatoriese kultuur deur ʼn magdom paradigmas en weliswaar gefragmenteerde
teorieë oorweldig is, was teoriebou in die ooreenstemmende literatuur oor gehalte in
hoër onderwys in die algemeen en oor die impak van eksterne gehalteversekering op
instellings in die besonder redelik skaars.
ʼn Kwalitatiewe gevallestudie is onderneem by ʼn universiteit van tegnologie wat onlangs
saamgesmelt het om twee aannames wat as vanselfsprekend aanvaar is, te ondersoek:
eerstens, dat organisatoriese kulture homogeen, unitêr en óm gedeelde waardes
gesentreer is en dat dit dus maklik gemanipuleer kan word (gewoonlik van bo af deur die
bestuur), en tweedens, dat die invoer van eksterne gehalteversekering ʼn
onproblematiese tegnologie is wat sonder teenspraak deur hoëronderwysinstellings
aanvaar sal word, aangesien dit op die prysenswaardige oogmerk van verbetering van die
gehalte van daardie instellings gegrond is. ʼn Konseptuele raamwerk bestaande uit vier
perspektiewe is ontwikkel vir die kritiese evaluering van die literatuur en dit verskaf die
grondslag vir die driedimensionele model wat vir die analise van die bevindings gebruik is.
Die navorsing het verskeie belangrike gevolgtrekkings na vore laat kom wat algemeen
geldende en duidelik bepaalde posisies ten opsigte van organisatoriese kultuur en
eksterne gehalteversekering blyk uit te daag. Eerstens moet organisatoriese kultuur
beskou word as efemeries eerder as konkreet, multidimensioneel eerder as enkelvoudig,
terwyl dit gelyktydig deur konflik, konsensus en onverskilligheid gekenmerk word en in ʼn
gedurige toestand van wisseling verkeer. Tweedens is eksterne gehalteversekering nie
noodwendig, soos in die vroeë konseptualisering en implementering belowe, ʼn
waardevrye en neutrale oefening gemik op verbetering van die gehalte van onderrig en
leer nie. Derdens kan veelvuldige kulture gelyktydig bestaan, met mekaar in interaksie
tree en mekaar voortdurend beïnvloed en natuurlik interaksies binne die organisasie en
die aard van betrokkenheid by inisiatiewe wat ekstern ontstaan, bepaal. Vierdens het
eksterne gehalteversekering oogmerke wat veel verder strek as die motiewe daarvan wat
dikwels moreel geregverdig en vir die openbare beswil is aangesien dit stilswyend en op
overte wyse optree as ʼn agent vir beheer, bemagtiging en transformasie en tegelyk as ʼn
agent van die regering, alhoewel nie noodwendig tot dieselfde mate nie.
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South African citrus farmers' perceptions of the benefits and costs of compliance with private sector certification schemes for citrus exports.Ndlovu, P. G. January 2010 (has links)
The main objective of this study was to analyse South African (SA) citrus farmers’ perceptions of the benefits and costs of complying with quality assurance (QA) certification schemes for citrus exports to the European Union (EU). The study used an e-mail and postal survey questionnaire mailed to a stratified random sample of 260 SA commercial citrus growers during July 2007. The survey yielded 108 usable responses - a response rate of 10.8% from the target population of 1001 commercial SA citrus growers. The main factors motivating respondents to adopt QA certification were to keep and maintain access to existing markets; to improve customer confidence in their products; to access new markets; and to meet food safety and retailer requirements. Principal Component Analysis (PCA)
identified six underlying dimensions of motivators, which suggest a drive by sampled respondents to gain certification to meet market requirements, achieve intra-farm benefits such as cost-reduction, and to remain competitive in existing and new foreign markets. The sampled respondents identified the main internal benefits from QA certification as the ability to retain existing markets; improved worker health and safety; better access to foreign markets; better farm organisation; and improved fruit safety
and orchard management. The PCA identified six broad dimensions of these internal benefits. Comparing the motivator and perceived benefit dimensions, most of the motivators seem to have been in part realised by the respondents. Respondents rated shared goals and values about the product; more joint decision making on fruit safety; more working together on quality assurance; a better business working relationship; improved
coordination; and improved trust as the six major supply chain benefits from QA certification. The two dimensions identified from these external benefits by PCA were: (1) Improved working relationship and product quality benefits, and (2) Improved cooperation and contractual benefits. The major costs of implementing EUREPGAP certification related to initial investment costs and the recurrent annual costs of compliance. The respondents, on average, spent an estimated R70655 on initial compliance
costs, mainly for infrastructure, additional buildings and employees training. Some 60% of respondents spent less than 1% of annual farm turnover on initial compliance costs, while most of the respondents (84%) spent less than 1% of annual farm turnover on recurrent costs of compliance. Growers that owned a pack-house had statistically significantly higher initial and annual costs of compliance. Most (63%) of the respondents had a relatively high level of overall satisfaction with QA certification. The second objective of this study was to analyse the determinants of SA citrus farmers’ overall level of satisfaction with QA certification. Ordinary Least Squares (OLS) regression estimated that perceived dimensions of internal benefits, namely (1) Foreign market access benefits; (2) Intra-farm benefits; (3) Improved fruit safety and orchard management; (4) Quality and worker welfare benefits; and (5) Ability to retain existing markets, all had a statistically significant positive influence on the sampled growers’ overall level of satisfaction with QA certification. Supply chain benefits also had a positive effect on overall level of satisfaction, although the effects were not
statistically significant. Similarly, no statistically significant relationship could be established between farm size or the respondents’ level of satisfaction with their certifying agents and their overall level of satisfaction with QA certification. Record keeping is required by nearly all EUREPGAP control chapters and for farm audits. Crop protection is also perceived as a complex requirement of the EUREPGAP protocol. Policymakers thus need to be aware of the extra costs that protocols create for management. The Citrus Growers’ Association of Southern Africa (CGA) could consider providing more extension advice to farmers on the technical requirements of certification (particularly best practices for implementing the control
chapters). Comparing the motivator and perceived benefit dimensions, most of the motivators for QA certification seem to have been in part realised by the respondents. For instance, the drivers to improve business image/market competitiveness/market access requirements/farm profitability were realised via perceived reputation/input cost savings/foreign market and profit improvement benefits. The study results, therefore, provide some evidence that QA certification is a necessary strategy for maintaining competitiveness in EU citrus markets. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2010.
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An exploration into the conditions enabling and constraining the implementation of quality assurance in higher education: the case of a small comprehensive university in South AfricaMasehela, Langutani Meriam January 2015 (has links)
At an international level, demands for accountability in respect of the quality of teaching and learning in higher education are increasing. This is also the case in South Africa. The response to these demands has taken the form of the introduction of quality assurance systems to higher education. In South Africa, a formal national external quality assurance was introduced to the higher education system in 2001 as a result of the establishment of the Higher Education Quality Committee. The Higher Education Quality Committee is a standing committee of the South African Council on Higher Education. Like other quality assurance agencies across the world, the Higher Education Quality Committee has the responsibility for i) auditing institutions of higher education and ii) accrediting learning programmes. The first cycle of institutional audits ran from 2004 until 2011. As quality assurance was introduced to the higher education system and the first cycle of institutional audits began, universities in South Africa developed policies and procedures intended to assure quality in three areas of their core functioning: research, teaching and learning and community engagement. The University of Venda, which is the focus of the study on which this thesis is based, was no exception. As a practitioner in the Centre for Higher Education Teaching and Learning at The University of Venda, it was my observation that the policies and procedures intended to assure quality in teaching and learning were not always implemented by academic staff members. This was in spite of poor student performance data which raised questions about the quality of the teaching and learning processes in place. The study underpinning this thesis was designed to explore this phenomenon. More specifically, it aimed to identify the conditions enabling and constraining the implementation of policies and procedures in two Schools in the University: the School of Health Sciences and the School of Human and Social Sciences. In order to explore these conditions, I adopted Roy Bhaskar’s Critical Realism as an under-labouring philosophy for the study. Critical realism posits a view of reality comprising three strata, none of which can be reducible to the other. The first of these strata is termed the level of the Empirical and consists of the experiences and observations which become apparent to us through the senses. The second layer, the Actual, consists of events from which these experiences and observations emerge. Underpinning both of these layers is a further layer, the Real, which is not accessible by empirical means and which consists of structures and mechanisms which generate both events at the level of the Actual and experiences and observation at the level of the Empirical. The design of my study sought to reach this deepest layer of reality to identify these mechanisms. Bhaskar’s critical realism is philosophy which needs to be operationalized using substantive, or explanatory, theory. For this purpose, I drew on Margaret Archer’s social realism. The design on my study drew on case study methodology and involved in-depth interviews with members of the two Schools which each formed cases within the more overarching case of the University itself. In addition to these interviews, I analysed a range of institutional documents related to the assurance of quality in teaching and learning. The exploration of enabling and constraining conditions at the level of the Real allow me to make a series of recommendations in the final Chapter of my thesis intended to enhance the quality assurance system introduced to the University.
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