ISO 13485 Medical Devices Quality Management System
Share on linkedin
Share on twitter
Share on facebook
Share on whatsapp
Share on email

ISO 13485

  • ISO Audit Toolkits

$499

ISO 13485 determines the requirements for the medical devices industry. This standard was established to be used by companies during the life cycle of medical devices, from production to post-production, including decommission and disposal.

Description

Reviews

There are no reviews yet.

Only logged in customers who have purchased this product may leave a review.

Testimonals
Crest Advisory Africa Logo
PECB Platinum Partner
The Institute of Risk Management South Africa
Services SETA