Clinical Regulatory Document Writing for Submission.

Our Work Speaks for Itself.

But our clients do a much better job explaining what that work means to their brands, their submissions, and to their bottom line.

Our Endorsements.

Here are just a few reasons why individuals and pharmaceutical organizations keep on working with us:

We have always had an excellent experience working with PreciseDox (formerly PRI). Their QC process and level of professionalism is unrivaled, and they have always delivered exactly what was expected.

VP, Clinical Development

We have used PRI continuously for the past 3 years for services. We don’t use their competitors, as they are our go to group. They have the expertise we require, and their ability to execute to the statement of work is where they really shine. We have a comfort level with the entire team.

Executive Director, Clinical Operations

I find them very easy to work with, and they know what they are doing. They are present, available, adaptable to change, and express their opinions to ultimately improve our final product. A very professional and personable organization.

Vice President, Clinical Development

I used PRI for regular medical writing, protocols, clinical study reports, IMPDs. PRI is the sole provider of medical writing services for our organization. They’re very collaborative. and not afraid to push back when appropriate. They point out risk vs quality. Finally, I have to say their QC services are outstanding!

Senior Global Clinical Program Director

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