Contact us:

Medical Device Documentation

We are experts in medical device-related documentation

We have many years of experience developing documentation for medical devices and medical diagnostic equipment. We understand FDA 801 guidelines and requirements for product labeling. We are experienced with complex electromechanical devices and related software.

We know how to "Write it, Right" when it comes to:

    • Instructions for Use (IFU)
    • Patient Manuals
    • Clinician Manuals
    • Quick-reference Guides
    • Quick-start Guides
    • Setup and Installation Manuals
    • Service and Maintenance Manuals and Procedures
    • Medical Device Software Documentation including online help systems
    • Directions for use
    • Inserts

We also have Quality and Regulatory Compliance experts who can assist you with

    • 510K submissions
    • Specific FDA labeling requirements
    • cGMP and ISO requirements and documentation

We are experienced with the software you use, including Adobe® FrameMaker® and InDesign®


We have writers who can do the research (Literature Route and/or Clinical Investigation Route) and develop your Clinical Evaluation Reports (CERs).

We also have experience developing Commissioning and Qualification (C&Q) Validation Documentation.

Having one company with the expertise to handle all the above lets you benefit from our team approach. Our writers can easily work closely with Quality and Compliance experts to ensure you get the best outcome.  

We also understand while you can fullfill the basic requirements that often doesn't mean the patient, medical professional, or lab worker is getting documentation that is easy to understand or use. Many companies' help lines are overused because their documentation is simply not being read because either the instructions are too difficult to follow or the information needed isn't readily found. We understand that and we draw upon our experience to develop and design documentation that is both easy to use and understand. Depending on the scope of the project, we can work with your human factors consultants or our's, and engage focus groups to ensure you are getting the best possible documentation through testing and verification.

If your products reach global markets, rest assured we also have the experience with translating and localizing documentation into as many as 21 different languages.

We can also develop training materials and marketing-related documention for your product.

Contact us at for a free consultation. Or call 1-800-985-7701. We will show you how to improve your content processes–and increase your productivity.

If you prefer, please feel free to fill out the form below and someone will contact you promptly.


Home | Site Map    Contact us:  [Toll-Free] 1-800-985-7701     
©2020 Precisely Write, Inc.    "Precisely Write" is a registered trademark of Precisely Write, Inc. All other trademarks and copyrights are the property of their respective owners.