GICRA offers additional services to facilitate international studies, also provides sponsors support in the following: Feasibility studies and patient access planning, Document translation
GICRA has a complete education system available for small companies looking to expand on training in Regulatory and Clinical compliance. We can also supply annual training on standard operating procedures and updating your company as needed.
The right data analysis is critical for study success. GICRA’s biostatisticians are committed to your success starting with a well-thought and carefully designed analysis plan all the way through to the analysis of study data.
We are committed to quality. We have quality assurance review processes in place for all stages of your product development and we conduct audits early and at measured intervals to identify and proactively limit any impact on your program.
Data Management is an integral component of GICRA’s global capabilities. We provide our clients with comprehensive data management plans prior to study initiation, along with on-going reporting.
We offers a full range of clinical study development and management services for all Phases (I, II, III and IV) of clinical research. All procedures are controlled by GICRA Standard Operating Procedures (SOPs).