Medical Device Technology Manufacturers Stay Up to Date

Software Solutions for Medical Device Innovators

The growth of wearables and smart, connected devices is ushering in a new era of patient-centric care. With 3-D printing, personalized medical device technology is now a reality. The convergence of the physical and digital worlds is here, now.

This new complexity also introduces new threats to profitability and increases the risk of recalls. It also underscores the ever growing need to address requirements of the FDA, EU MDR, and other regulatory bodies. Stay up to date on latest articles, reports, and blogs.

EU MDR and What it Means for Life Sciences

The European Union Medical Device Regulation (EU MDR) is the most significant revision to the EU regulatory system in over 20 years. If you’re like most medical innovators – still searching for a workable solution – PTC can help.

Find Out More About the Regulations

Preparing for EU MDR Product Submissions: A Sustainable Approach

This guide covers all the essential details you need to understand the data requirements of EU MDR product submissions and how to comply.

Read The EU MDR eBook

Medical Device Research Survey

The Impact of IoMT on Patient Outcomes: Changing the Business of Healthcare in the Outcome Economy

Medical Devices Research Survey

Close the Quality Gap with Modern Closed-Loop Processes

New Axendia Research: Drive a Culture of Quality Within the Medical Device Manufacturing Ecosystem

Read the Report

The Impact of Medical Device Recalls and How to Avoid Them

With investments in the right technology, your company is better positioned to ensure quality and avoid costly recalls.

Read the Blog

2019 Medical Devices Manufacturers Software Selection Guide

This independent guide identifies the critical challenges, key capabilities, and vendor selection criteria needed to choose the right medical device technology.

Read the Tech-Clarity Software Selection Guide

Four Ways Medical Device Companies Can Become More Profitable

Focusing on four key areas, medical device companies improve competitiveness and boost profitability.

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FDA And The Case For Quality For Medical Device Manufacturers

Know the risks and the standards for successful FDA audits.

The FDA - Find out More

European Medical Technology - A €100 Billion Opportunity

Know the consequences of negligence and why you should understand ISO 13485.

ISO 13845 - Find out More

How Medical Device Manufacturers Optimize the Risk/Benefit Ratio Over the Product Lifecycle

A product-centric approach makes it possible to easily propagate changes across the entire lifecycle, from design to manufacturing.

Read the Benefits of a Product-Centric Approach

Deliver Innovative Products to Market Quickly with Controlled Processes for Quality

According to Aberdeen, using a combination of PLM and Quality Management systems can lower internal and external failures by 50%.

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2017 Axendia Report: Managing Medical Devices Across The Total Lifecycle

Staying on the right side of compliance and quality requires rethinking old strategies.

Read the Report


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