AAMI TIR97:2019

HOME
PRODUCTS
HELP
Glossary

Principles for medical device security - Postmarket risk management for device manufacturers

Provides guidance on methods to perform postmarket security risk management for a medical device in the context of the Safety Risk Management process required by ISO 14971. This TIR is intended to be used in conjunction with AAMI TIR57:2016.

ADD TO ALERT
PDF

ADD TO ALERT

Please first log in with a verified email before subscribing to alerts.

Your Alert Profile lists the documents that will be monitored. If the document is revised or amended, you will be notified by email. You may delete a document from your Alert Profile at any time. To add a document to your Profile Alert, search for the document and click “alert me”.

ADD TO ALERT

Please first verify your email before subscribing to alerts.

ADD ALERT

Already Subscribed to this document.

PDF DOCUMENT FORMAT

Documents sold on the ANSI Webstore are in electronic Adobe Acrobat PDF format.

DRM PROTECTED DOCUMENTS

Some PDF files are protected by Digital Rights Management (DRM) at the request of the copyright holder. You can download and open this file to your own computer but DRM prevents opening this file on another computer, including a networked server. Some copyright holders may impose other restrictions that limit document printing and copy/paste of documents.

NON PRINTABLE DOCUMENTS

Those documents cannot be printed at the request of the copyright holder.

CONTENT PROVIDER
Association for the Advancement of Medical Instrumentation [aami]

Historical

Principles for medical device security - Postmarket risk management for device manufacturers

Useful Links

CUSTOMER SERVICE

Our Contacts

Historical

AAMI TIR97:2019

Principles for medical device security - Postmarket risk management for device manufacturers

Are the documents at the ANSI Webstore in electronic Adobe Acrobat PDF format only?

Useful Links

CUSTOMER SERVICE

Our Contacts