SIST EN ISO 14155:2020

Oznaka standarda: SIST EN ISO 14155:2020
Koda projekta: 00206077
Organizacija: SIST
Naslov (angleški): Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
Naslov (slovenski): Klinične raziskave medicinskih pripomočkov za ljudi - Dobre klinične prakse (ISO 14155:2020)
Če kupite standardizacijski dokument v .pdf formatu prek spletne prodaje, vam nudimo 10% popust pri spodnji ceni brez DDV. Cenik SIST
Dokumenti
Ime Jezik Status Cena Dodaj v košarico
SIST EN ISO 14155:2020 angleški jezik Active SIST-M: 119.79 EUR
PDF
Papir
Tehnični odbor: VAZ - Varovanje zdravja
ICS: 11.040.01
Status: Objavljen
Objavljen: 01-okt-2020
Refer. št. objave: Sporocila 2020-10
Referenčna oznaka: EN ISO 14155:2020
Področje projekta (angleško): This document addresses good clinical practice for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the clinical performance or effectiveness and safety of medical devices. For post-market clinical investigations, the principles set forth in this document are intended to be followed as far as relevant, considering the nature of the clinical investigation (see Annex I). This document specifies general requirements intended to — protect the rights, safety and well-being of human subjects, — ensure the scientific conduct of the clinical investigation and the credibility of the clinical investigation results, — define the responsibilities of the sponsor and principal investigator, and — assist sponsors, investigators, ethics committees, regulatory authorities and other bodies involved in the conformity assessment of medical devices. NOTE 1 Users of this document need to consider whether other standards and/or national requirements also apply to the investigational device(s) under consideration or the clinical investigation. If differences in requirements exist, the most stringent apply. NOTE 2 For Software as a Medical Device (SaMD) demonstration of the analytical validity (the SaMD’s output is accurate for a given input), and where appropriate, the scientific validity (the SaMD’s output is associated to the intended clinical condition/physiological state), and clinical performance (the SaMD’s output yields a clinically meaningful association to the target use) of the SaMD, the requirements of this document apply as far as relevant (see Reference [4]). Justifications for exemptions from this document can consider the uniqueness of indirect contact between subjects and the SaMD. This document does not apply to in vitro diagnostic medical devices. However, there can be situations, dependent on the device and national or regional requirements, where users of this document might consider whether specific sections and/or requirements of this document could be applicable.
Povezava na standarde
Povezava Ime Datum
Nadomešča SIST EN ISO 14155:2012 - Klinične raziskave medicinskih pripomočkov za ljudi - Dobre klinične prakse (ISO 14155:2011) 01-okt-2020
Nadomešča SIST EN ISO 14155:2011/AC:2011 - Klinične raziskave medicinskih pripomočkov za ljudi - Dobre klinične prakse - Tehnični popravek 1 (ISO 14155:2011/Cor 1:2011) 01-okt-2020


• Slovenski standardi SIST s cenovnim razredom AC so popravki standardov in so v večini primerov brezplačni.

• Slovenski standardi SIST s cenovnim razredom AP so privzeti tuji standardi, katerih sestavni del je izvirni standard, ki ga moramo pridobiti pri izdajatelju v tujini. Naročilo pošljite na: prodaja@sist.si.

Najbolje prodajani standardi