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Simplify your drug submission process

A boutique CRO – specialized in the documents that define your data.

We Can Help
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1. Regulatory Writing

We specialize in submission-ready regulatory documents that meet global agency standards. Our writers know what matters to reviewers – clarity, consistency, and accuracy.

2. Quality Control

Quality is built into every stage of our process, not tacked on at the end. Our QC reviewers ensure that every data point, cross-reference, and citation is accurate and consistent. Our goal is simple: eliminate errors before they become problems.

3. Publishing

We take final documents across the finish line. From formatting and navigation to eCTD compliance, we make sure your documents are submission-ready.

What we do.

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Why CDM?

At CDM, we understand the importance of communication. Our commitment is to offer unparalleled services and unwavering customer support in the effort of improving health outcomes across the world.

Our commitment to you.

Quality Matters

Improve your content by working with a team who understands the importance of quality through every step of the process.

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Customers Matter

Work with us to develop a solution that meets your needs. Each project is special and unique. Treat it that way!

Trust Matters

You know what's not fun?  Missing deadlines. Painstaking revisions. And a lack of confidence in your partners. Let's breathe some life back into your process!

Contact Us

Headquarters:

Fort Washington, PA 19034

United States

215-643-2006

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© 2025 CDM Consulting

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