Iso 14155

Author:Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 29.10.2020

Dieser Artikel auf Deutsch

Synonym(s)

International Organization for Standardization

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

HistoryThis section has been translated automatically.

ISO 14155 is the European standard for medical devices from the International Organization for Standardization (ISO) and corresponds to an adapted guideline of GCP (Good Clinical Practise) for clinical studies with medical devices.

General informationThis section has been translated automatically.

ISO 14155 sets out requirements for the protection of the volunteer and includes guidelines for the development, conduct, recording and reporting of clinical trials that serve as a basis for evaluating the safety or performance of medical devices. In the current version of 2011 there are changes to the previous versions in the definition of safety and product defects

ISO 14155 guarantees the safety and rights of the study participants, controls the study quality, supports all parties involved in a study, regulates risk management and defines the responsibilities of the sponsor, monitor (Clinical Research Associate) and the investigator. It also regulates the contents of the investigator brochure and defines the documents that should be available at the study site and in the sponsor's files.

Authors

Last updated on: 29.10.2020