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.
We offer extensive industry experience shaping project plans to meet diverse regulatory requirements.
We work with our clients to thoroughly understand the study objectives, parameters and protocol.
Country feasibility, site and investigator selections are crucial steps for any clinical trials, as it impacts the study for its whole duration.
At CRU-GLOBAL, we have a flexible structure to maintain the quality of the whole process untouched.
Auditing is a valuable tool to gain insight into the performance of your vendors, confirm you have oversight and assure inspection readiness.
CRU-GLOBAL appoints a clinical project manager to be the team leader for each clinical study.
We can help on ever activity for data planning and management involved on the development of clinical trials and statistical analysis.