What we do

Simply put, Full Spectrum gets your medical device or life sciences instrument to market.
We have extensive experience organizing and transporting data from regulated devices
to wherever it needs to go — mobile devices, cloud apps/backend, AI/ML, EMR, you name it!
This includes handling all the required documentation of Regulated Systems for FDA Submission.
And with a team of Engineering and R&D specialists skilled across the entire product
development lifecycle, we’re ready to work with you at any stage.
From initial strategy to program recovery, and everywhere in between. 

And with a team of Engineering and R&D specialists skilled across the entire product development lifecycle,
we’re ready to work with you at any stage. From initial strategy to program recovery, and everywhere in between.

Full Spectrum’s Advantage:

Industry Innovators since 1982
Leverage our experience and know-how to accelerate your product to market

Exceptional Regulated Product Development Expertise
We know how to balance between adherence to process and urgency of getting to market – make compliance an asset

Flexible Engagement Models
Blending the strengths and efficiencies of your team with ours to reduce development risk and increase velocity

Why Partner with Full Spectrum

Since 1982, the team at Full Spectrum has been leading the way to one breakthrough
after another in the advancement of medical and life science technology.
We know the regulatory ins-and-outs better than most.
And with hundreds of development efforts under our belts, we know how to get things done.
Quickly. Efficiently. Collaboratively.