Our recruitment process includes an ongoing general campaign as well as study specific recruitment strategies to ensure that our panels are filled as quickly and efficiently as possible.
e-CRF design and maintaince, maintainance of data base under FDA approved with full audit trail
We have developed a strong reputation for delivering a high quality, reliable and responsive randomisation writing service
CRS offers statistical analysis of medicinal products and clinical development programs.
Our experienced Project Management team has extensive expertise in managing clinical trials across a wide range of therapeutic areas and utilizing numerous study design
Team of Data Managers and top experts Statisticians designs, builds, and deploys clinical database that meets industry standards in regards to timelines and quality
Our team of Investigators and Nurses ensure participant’s safety at all times during the course of the clinical trial
CRS provides over 20 years of Clinical research experience with management team supporting clinical trials in our region
We are committed to the health, safety and well-being of participants.