Critical Path Research

Comprehensive Proficient Reliable

Who Are We And what do we do ? . . .

High above the fray, let our highly skilled professionals with more than 200 years of combined experience put you on the straight path with any aspect of clinical research.

Call us with your research project needs. This is what we can do for you:

  • Study Start Up
  • All Study Related Reports & Documents
  • Regulatory Supervision
  • Medical Writing
  • Auditing
  • Training

Therapeutic Areas in Phases I - IV:

  • Oncology
  • Neurology
  • Cardiology
  • Respiratory
  • Endocrinology
  • Surgical
  • Special Senses

Our turnaround time will be met masterfully, comprehensively and in compliance with all regulations.

CPR will always be available in an advisory capacity to respond to your questions and issues in a timely manner. Our goal is to make your group autonomous well beyond the scope of your project.

If you give a man a fish, he eats for a day. If you teach that man to fish, he eats for life !!!!


At some stage it may be imperative to receive professional guidance in order to follow the appropriate path for Federal and Global compliance involving all processes and procedures in clinical research.

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Auditing should not be a panic - You have been trained as required, with all the necessary documents and directives. Auditing will test your powers of implementation and how management has taken charge of ensuring that the processes and procedures have been implemented. The cohesive evidence is in preparing for an Audit

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Medical Writing

During the course of your project, you may require assistance with various documents or specific services to help you through your Project voyage.

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We can help your staff better understand the “required” code of Federal Regulations and the ICH-GCP Guidelines as it applies to all aspects of Clinical Research.
Any and All are available for review and training.

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