National Repository of Grey Literature 3 records found  Search took 0.02 seconds. 
Analysis of conformity assessment procedure of a hammer
Úlehlová, Eva ; Slažanský, Martin (referee) ; Harčarík, Matej (advisor)
This bachelor thesis deals with the analysis of the conformity assessment procedure of a hammer with its specification. The work is focused on a revolver hammer and was developed in cooperation with a company producing revolvers. In addition to describing and analyzing the hammer’s specification and conformity assessment procedure, the aim of the work was also to propose improvements. The theoretical part deals with the principles for prescribing the required product geometry on technical drawings. The output of the thesis is a proposal to improve the specification and a proposal to modify the conformity assessment procedure.
Analysis of conformity assessment procedure of a hammer
Úlehlová, Eva ; Slažanský, Martin (referee) ; Harčarík, Matej (advisor)
This bachelor thesis deals with the analysis of the conformity assessment procedure of a hammer with its specification. The work is focused on a revolver hammer and was developed in cooperation with a company producing revolvers. In addition to describing and analyzing the hammer’s specification and conformity assessment procedure, the aim of the work was also to propose improvements. The theoretical part deals with the principles for prescribing the required product geometry on technical drawings. The output of the thesis is a proposal to improve the specification and a proposal to modify the conformity assessment procedure.
Launching medical devices on the market
Dvořáková, Jitka ; Svoboda, Petr (advisor) ; Millerová, Ivana (referee)
The issue of launching medical devices on the market became more intense in the last few decades in connection to the expansion of the pharmaceutical industry and legal area. This legal area is still mostly undescribed and it stands in the shadow of known and more discussed medical products. Proper legal theoretical analysis is often completely absent. This master thesis aims to complexly describe and analyse theoretical bases of current legislative regulating the launching of the medical devices on the market, including other processes related to this issue. Emphasis is places on the concept of medical device, the responsibility of the manufacturer and the nature of notified body. The author focuses on the subsequent conformity assessment process and process of registration. The process of notification and exemption from this obligation and administrative nature of selected documents. The thesis is divided into eleven chapters and the introductory chapter focuses on a general introduction to the field of pharmaceutical law, namely the regulation of medical devices, including the definition of basic questions in the work under study. The second chapter deals with the analysis of sources of legal regulation of medical devices. The chapter is divided into sources of the law of the Czech Republic and...

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