CRO Services
Due to the increasing need from our study sponsors – especially in early phase studies – CRU-GLOBAL developed its own CRO department and services for pharmaceutical and MedTech industry. CRU-GLOBAL is able to conduct all study related activities with its own permanent staff, and in very special cases with CRU-GLOBAL’s regular external consultants.
Regulatory
We offer extensive industry experience shaping project plans to meet diverse regulatory requirements.
Study Planning
We work with our clients to thoroughly understand the study objectives, parameters and protocol.
Monitoring
At CRU-GLOBAL, we have a flexible structure to maintain the quality of the whole process untouched.
Feasibility & Site Selection
Country feasibility, site and investigator selections are crucial steps for any clinical trials, as it impacts the study for its whole duration.
Auditing
Auditing is a valuable tool to gain insight into the performance of your vendors, confirm you have oversight and assure inspection readiness.
Project Management
CRU-GLOBAL appoints a clinical project manager to be the team leader for each clinical study.
Data Management & Biostatistics
We provide comprehensive support for all aspects of data planning and management throughout clinical trial development, including statistical analysis.