New regulations in the field of medical devices
Aage limits for biochemists biologists or chemists in the medical system and the condition of holding the title of Doctor of Sciences in order to continue working in private health facilities which represents the denial of freedom of exercise of the profession without having any objective and rational justification thus leading to the violation of the provisions of art. para. of the Constitution regarding the fundamental right to work. As for the criticism of unconstitutionality related to art. of the Constitution regarding the restriction of the exercise of certain rights or freedoms the Court finds that its analysis is no longer necessary since the violation of the right to work has been observed.Leave a reply Your email address will not be published. Mandatory fields are Country Email List marked with Comment Name Email Site web Save my name email and website in this browser for the next time I comment. Site web Save my name email and website in this browser forIT minutes AnaMaria Udriste April On April the Medical Devices Regulation and the In Vitro Diagnostic Medical Devices Regulation were officially adopted. These regulations will amend and unify the European legal framework for medical devices adjusting to new technologies applied in the medical sector and replacing the three directives currently applicable.
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The rules emphasize the importance of the safety of medical devices and their use. As these regulations contain various new obligations it will be very important that all actors involved examine and implement them very carefully. Introduction The current legal framework for medical devices in the European Union is based on the following directives adopted in the s Directive EEC active implantable medical devices Directive EEC medical devices Directive EC medical devices for in vitro diagnosis These directives have been implemented in the Member States by national legislation. Since the adoption of these directives technology has not stood.
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