EN ISO 14155-1:2009

Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003)

Publication date:   Sep 16, 2010

General information

99.60 Withdrawal effective   Feb 1, 2011

CEN

CEN/TC 258 Clinical investigation of medical devices

European Norm

11.100.20   Biological evaluation of medical devices

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Scope

ISO 14155-1:2002 defines procedures for the conduct and performance of clinical investigations of medical devices. It specifies general requirements intended to:
protect human subjects;ensure the scientific conduct of the clinical investigation;assist sponsors, monitors, investigators, ethics committees, regulatory authorities and bodies involved in the conformity assessment of medical devices.
ISO 14155-1:2002
specifies requirements for the conduct of a clinical investigation such that it establishes the performance of the medical device during the clinical investigation intended to mimic normal clinical use, reveals adverse events under normal conditions of use, and permits assessment of the acceptable risks having regard to the intended performance of the medical device,specifies requirements for the organization, conduct, monitoring, data collection and documentation of the clinical investigation of a medical device,is applicable to all clinical investigation(s) of medical devices whose clinical performance and safety is being assessed in human subjects.
ISO 14155-1:2002 is not applicable to in vitro diagnostic medical devices.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Harmonized/Supporting
90/385/EEC

Active implantable medical devices

Harmonized/Supporting
2007/47/EC

Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market

Life cycle

PREVIOUSLY

WITHDRAWN
EN ISO 14155-1:2003

NOW

WITHDRAWN
EN ISO 14155-1:2009
99.60 Withdrawal effective
Feb 1, 2011

REVISED BY

WITHDRAWN
EN ISO 14155:2011

Relations

Adopted from ISO 14155-1:2003 IDENTICAL