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The scientific methodologies in these papers differ greatly.
In addition to these regulatory changes, government agencies have been active in establishing projects—either alone, or in collaboration with pharmaceutical companies and other bodies with the aim of improving the quality of pharmacovigilance and pharmacoepidemiology and of exploring and developing new methodologies in these fields.
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The lack of that requirement suggests the use of agile methodologies, justifying the use of these methodologies in the present work [15].
The main drawback of these methodologies in the industrial environment is the number of tuning parameters to be selected.
3 4 However to date, there has been little exploration of these methodologies in the clinical setting.
Application of these methodologies in the area of infection diseases is, however, still limited and much work is to be done to popularise them.
We discuss their applicability, possible options available to policy makers and the difficulties and potential pitfalls in implementing these methodologies in the frame of the currently existing policy framework in the European Union.
We discuss the possible options available to policy makers and the difficulties and potential pitfalls in implementing these methodologies in the frame of the currently existing policy framework in the European Union.
The implementation of these methodologies in the cardiovascular field will certainly help to answer the above questions and, thus, to shed light on the epigenetic events underlying transcription changes that accompany heart failure.
A comparison between these three methodologies in the integrative analysis of mRNA and protein abundance from a study of Plasmodium falciparum is included in this supplement [ 34].
The purpose here was to start the process of developing standardized and better methodology in these studies.
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