August 8, 2017
Irvine, California Great Park: Palm Court

Irvine Medical Device Development: The Choice Is Yours

You’re located in Irvine and you have sketched out a great new medical device idea. Maybe you are a start-up, but more than likely you have an established company and your current R&D team simply doesn’t have the band-width or special skills needed to bring your idea to life. Selecting a medical device engineering team to work with your existing Irvine team may seem daunting – but look no further than Murrieta, where REV.1 Engineering […]
August 3, 2017
Carlsbad, CA medical device companies

Attention Carlsbad Medical Device Companies: Discover Murrieta Research & Development Services

If your company is based in Carlsbad, CA and you are looking to outsource your medical device development, look no further than REV.1 Engineering in Murrieta. You are invited to visit our state-of-the-art facilities and meet with our team about your latest medical device project. Whether you have a napkin sketch of an idea or a prototype that you can’t seem to move to the next phase, we are ready to get started today. Our […]
July 31, 2017
Foothill Ranch CA Map

Foothill Ranch Medical Device Development: Rapid Transformation from Prototype to Commercialization

Getting a new medical device product to market is a challenge. If your company is located in Foothill Ranch, read on to learn more about REV.1 Engineering, a top outsource solution for medical device development located in nearby Murrieta. Our streamlined and effective product development and project management process operates in a unique and proprietary ecosystem that has moved our clients’ medical devices from napkin sketch to prototype to manufacturing. Your Dedicated, Experienced Team With […]
July 11, 2017
Medical Device Development - Quality Engineering

The Second Pillar of Medical Device Engineering: Creating an Effective Quality System

In our last blog, we explored Design Control – the first of three pillars that support quality medical device development. The second pillar is the creation of a Quality System. This pillar is instrumental in meeting regulatory requirements to FDA and CE Mark agencies requiring compliance to ISO 13485 – Medical Devices Quality Management System and ISO 9001 – Quality Management System. Regulatory entities require that the framework of a quality system be compliant to […]
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