Comprehensive Clinical Research Solutions

Our Core Capabilities

Planning & Study Design

We provide expert support in designing your clinical trial to align with regulations and study goals:

  • Clinical research design, development, and validation

  • Protocol development for FDA registries and clinical trials

  • Preparation and submission of FDA IND (Investigational New Drug) and IDE (Investigational Device Exemption) applications

  • Design and/or management of electronic databases and creation of Case Report Forms (eCRFs)

  • Site selection and feasibility assessments

  • Investigator qualification and selection to ensure strong site leadership

Study Maintenance & Oversight

We maintain high-quality execution throughout your trial with continuous oversight and support:

  • Clinical monitoring, including routine site visits

  • Audit preparation for sponsors or FDA inspections

  • Data management and statistical analysis

  • Site closeout preparation and execution

Trial Initiation

Our team ensures a smooth launch with strategic planning and regulatory compliance:

  • Development and negotiation of clinical trial budgets

  • Planning and execution of investigator meetings

  • Conducting site initiation visits (SIVs)

  • Regulatory compliance in accordance with GCP (Good Clinical Practice) guidelines

Additional Services

We also provide specialized support services to help maximize your trial’s impact and success:

  • Manuscript preparation and submission for publication

  • Teaching and educational support for staff or sites

  • Temporary staffing solutions for clinical research roles

  • Spanish-language translation of informed consent documents

At Comprehensive Research Associates, we specialize in delivering end-to-end clinical research services tailored to the unique needs of biotechnology firms, academic institutions, medical device companies, and pharmaceutical organizations. Our seasoned team ensures that each project is executed with precision, integrity, and adherence to regulatory standards.

With over 20 years of experience in designing and managing hundreds of successful clinical trials, Dr. Frank Peacock leads CRA with a proven track record of excellence in clinical research. His ability to structure trials that reliably meet clinical endpoints sets CRA apart in the field.