Imagine not having to worry about the traceability of regulatory requirements down to product parts. What if you had access to early insights into product behavior that helped optimize patient outcomes? What if you could also reduce the cost of compliance and quality?
Sounds like mission impossible, right?Read the Tech-Clarity Software Selection Guide for Medical Device Manufacturers.
Balancing regulatory complexity, quality requirements and profitability while continuously striving to manufacture innovative products is not easy. To complicate matters, digital transformation initiatives force medical device companies to rethink entire processes and even their corporate culture.
We can’t change the rules of the game, but we can choose the best, smartest move. Though it was sometimes seen as an inconvenient IT burden in the past, PLM is in fact your springboard to digital transformation.
With the right PLM solution, you can start the transition from viewing every process in an isolated manner to embracing a closed-loop approach. Directly integrating regulatory workflows as early as possible in your design process and reviewing them in an agile way across the product development stage is the first step to your new quality backbone.
Read the e-book Awareness Unlocks Potential to understand how PTC can help you easily improve designs, documentation, communication, quality, and service.
Download the 2017 Axendia Report: Managing Medical Devices Across the Total Lifecycle to find out why the shift from reactive compliance reporting to proactive quality management is the key to success for medical device manufacturers.
If you’re interested in learning more about top medical industry disruptors and firsthand insights into ways to address common industry obstacles, watch this on-demand webinar. In it, life sciences industry analyst firm Axendia highlights how medical device companies use technology to support a culture of innovation and quality.