Welcome to Precision Research, Inc.
a Contract Research Organization Specializing in Medical Writing

The professional Medical Writing Group at Precision Research, Inc. provides leadership in regulatory submission planning and help with additional document needs. Our knowledge of regulatory guidances for medical writing of regulatory submission documents is proven in numerous therapeutic areas. Regulatory submission planning requires knowledge of clinical research and development, and our Medical Writing Group collectively has over 50 years of experience.

The highest quality medical writing requires close interaction and strong communication, along with accuracy and attention to detail. Our medical writers establish strong communication links with the physicians, statisticians, and regulatory representatives and interact often during regulatory submission planning. They become part of your clinical team, attending all meetings for clinical study reports, regulatory submission documents, and additional clinical documentation. Efficient and organized medical writing utilizes templates for clinical study reports and regulatory submission documents, and our Medical Writing Group has decades of hands-on experience. Accuracy and attention to detail in all of our clinical study reports and regulatory submission documents are ensured by our competent and extremely experienced quality control group .

Do you have tight timelines? Contact our Medical Writing Group now to begin your regulatory submission planning, including early medical writing for protocols, clinical study reports and regulatory submission documents. With Precision Research, Inc., there's no reason not to have the quality medical writing help you need!

Experience in Therapeutic Areas

Briefing Documents

Clinical Overview

Clinical Protocols

Clinical Study Reports
(Phase 1, 2, 3, and 4)

Integrated Summary of Efficacy

Integrated Summary of Safety

Investigator Brochures

Patient Narratives

Summary of Clinical Efficacy
(section 2.7.3)

Summary of Clinical Safety
(section 2.7.4)

Summary of Clinical Pharmacology
(section 2.7.2)


Medical Writing

PRI writers have experience with INDs, NDAs, and BLAs.

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Quality Control

Review our Quality Control capabilities for documents and data.

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Do you have the qualifications to be a member of the PRI team?

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