---
product_id: 47603156
title: "Managing Medical Devices within a Regulatory Framework"
price: "COP 708137"
currency: COP
in_stock: true
url: https://www.desertcart.co/products/47603156-managing-medical-devices-within-a-regulatory-framework
store_origin: CO
region: Colombia
---

# Managing Medical Devices within a Regulatory Framework

**Price:** COP 708137
**Availability:** ✅ In Stock

## Quick Answers

- **What is this?** Managing Medical Devices within a Regulatory Framework
- **How much does it cost?** COP 708137 with free shipping
- **Is it available?** Yes, in stock and ready to ship
- **Where can I buy it?** [www.desertcart.co](https://www.desertcart.co/products/47603156-managing-medical-devices-within-a-regulatory-framework)

## Best For

- Customers looking for quality international products

## Why This Product

- Free international shipping included
- Worldwide delivery with tracking
- 15-day hassle-free returns

## Description

Managing Medical Devices within a Regulatory Framework helps administrators, designers, manufacturers, clinical engineers, and biomedical support staff to navigate worldwide regulation, carefully consider the parameters for medical equipment patient safety, anticipate problems with equipment, and efficiently manage medical device acquisition budgets throughout the total product life cycle. This contributed book contains perspectives from industry professionals and academics providing a comprehensive look at health technology management (HTM) best practices for medical records management, interoperability between and among devices outside of healthcare, and the dynamics of implementation of new devices. Various chapters advise on how to achieve patient confidentiality compliance for medical devices and their software, discuss legal issues surrounding device use in the hospital environment of care, the impact of device failures on patient safety, methods to advance skillsets for HTM professionals, and resources to assess digital technology. The authors bring forth relevant challenges and demonstrate how management can foster increased clinical and non-clinical collaboration to enhance patient outcomes and the bottom line by translating the regulatory impact on operational requirements. Covers compliance with FDA and CE regulations, plus EU directives for service and maintenance of medical devices Provides operational and clinical practice recommendations in regard to regulatory changes for risk management Discusses best practices for equipment procurement and maintenance Provides guidance on dealing with the challenge of medical records management and compliance with patient confidentiality using information from medical devices

## Technical Specifications

| Specification | Value |
|---------------|-------|
| Best Sellers Rank | #6,383,930 in Books ( See Top 100 in Books ) #856 in Commercial Business Law #994 in Medical Technology (Books) |
| Customer Reviews | 3.8 out of 5 stars 3 Reviews |

## Images

![Managing Medical Devices within a Regulatory Framework - Image 1](https://m.media-amazon.com/images/I/715atiMGfNL.jpg)

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*Product available on Desertcart Colombia*
*Store origin: CO*
*Last updated: 2026-10-19*