Services
Regulated Business Transformation
Stacks of paper weighing you down? Different processes at each of your locations globally? Let us help you move that stack to archives. We have helped global pharmaceutical companies analyze, map, and mind the gap, then standardize and move to fully electronic processes. In many instances this includes automating a number of processes in their Quality Management System (QMS). We are the practical consulting solution to increase your GCP compliance and efficiency, and incorporate risk management practices from a variety of industries to your risk-based clinical research program.
Clinical Research Oversight and Management
Need contract consultant staffing to project manage your clinical trial, or a CRA to step in and clean up a study or do it correctly the first time? Consulting CRAs, Certified Project Managers, Trainers, or an experienced GCP Auditor to help bring problem sites (or staff) up to speed are all available for short or long term projects. Make your clinical research efficient.
Quality and Audit
Are your sites under control? How do you know? Consulting Auditors with experience on both sides of the table know where to look, and how to find the correct string to pull that identifies your risk. Assure compliance in your clinical research program today.