Clinical Regulatory Document Writing for Submission.

PreciseDox writes regulatory documents for Pharmaceutical and Biotechnology companies throughout the world. Our quality control team conducts a thorough review of each document to ensure accuracy and consistency for submission.


We are proven leaders, and valued partners, in the medical writing community. Our decades of experience span all aspects of regulatory submissions.


PreciseDox senior medical writers understand and explain complex data in ways that provide context, insights, and value to clinical trial results.


PreciseDox medical writing and quality control professionals work in tandem to provide final documents that accurately reflect the study data.


PreciseDox team of experienced medical writers respect and consistently meet the milestones of our Pharmaceutical and Biotech clients.


The PreciseDox team of senior medical writers has a proven reputation for excellence that builds successful, long-term, client relationships.

“I’ve worked with PreciseDox for over 15 years now. They’re flexible and realistic when it comes to determining the scope of every project. We don’t use competitors. They’re our only go-to group.”

Vice President, Clinical Operations and Project Management

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To learn more about how we can help your organization or request a quotation, please call us at 610-296-1747.