Streamlining Documentation Services

Properly documenting your solution now will save you money later.

To ensure traceability, documentation for software as a medical device must meet strict regulatory guidelines and deliverables in order to demonstrate readiness for actual use. The written information accompanying a software product must be clear, concise, and meet stakeholder needs. We have dedicated specialists representing all stages of the software development lifecycle who are well-versed in developing documentation that adheres to the highest standards.


Skills

Comprehensive documentation for product planning, release, and everything in between

A wealth of experience in preparing paperwork for various regulatory agencies, including the U.S. Food and Drug Administration (FDA)

Full development teams fluent in English and a team of translators to cover major European languages

Active knowledge of all the major tools and methods for producing, reviewing, approving, and maintaining product documentation during and after the development process

Are You Ready for a Solution?

This is a perfect opportunity to find the solution to your problems. Please feel free to request a free 30 minute consultation..

Are You Ready for a Solution?

This is a perfect opportunity to find the solution to your problems. Please feel free to request a free 30 minute consultation..
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Connect With Us

Our Offices

Office In the US :

1039 Chrome Rd.
Oxford, PA 19363
Office In Hungary:

Vasvári Pál u. 1/C
H-9024 Győr
+36-96-550-521