We are a team of experienced regulatory and medical writers dedicated to helping medical device and technology manufacturers meet regulatory body requirements by providing unparalleled support through documentation initiation and maintenance.
We offer a wide range of writing services, including regulatory writing, clinical study, research-based writing, project management, and training and education. Whether you need one-off pieces or ongoing help, we are here for you!
As a boutique organization, we work closely with our clients to understand their unique needs and goals. From there, we develop a strategy that aligns with their goals and requirements. Our writers then get to work creating high-quality documentation that meets those goals.
"Your team is one of the best we've worked with. You all hit the ground running, and we were able to complete CEPs and CERs with very tight deadlines. I'm excited for our next project together!"
"The MedTech Writing and Consulting project manager consultant taught us how to structure our priorities and instill best practices to better our team. We would not have been able to streamline our process without their help."
"We could not have completed these notified body responses without you, especially with the aggressive deadline we were facing. Thank you!"
"The training taught me everything I needed to know to become an asset to my team as a medical writer. I feel comfortable at my position and am grateful to learn from the best!"
MedTech Writing and Consulting
Copyright © 2024 MedTech Writing and Consulting - All Rights Reserved.
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.
..and let us handle your ongoing Post-Market Surveillance. See how your device (and similar devices) are operating out in the market!