![](https://www.brd.co.il/wp-content/uploads/2019/06/735862213.jpg)
Clinical Project Management
Throughout the years of its operation B.R.D CRO has gained extensive experience in a broad range of therapeutic areas and has established strong working relationships with the leading physicians in their field, in most medical centers and health care clinics across Israel.
![](https://www.brd.co.il/wp-content/uploads/2019/06/70867792.jpg)
Medical Writing
Medical writing is an integral part of clinical research and involves creating well-structured scientific and regulatory compliant documents that plays a critical role in the success of clinical trial submissions.
![](https://www.brd.co.il/wp-content/uploads/2019/06/606977243.jpg)
Clinical Operations
A qualified experienced clinical operations team is an essential key to the delivery of smoothly running clinical trials in accordance with ICH-GCP Guideline (or ISO 14155 for Medical devices), the approved study protocol and the local MOH requirements.
![](https://www.brd.co.il/wp-content/uploads/2019/06/532873330.jpg)
Data Management
Clinical Data Management (CDM) is a critical phase in clinical research, which leads to collection and generation of high-quality, reliable, and statistically sound data from clinical trials.
![](https://www.brd.co.il/wp-content/uploads/2019/06/721950199.jpg)
Regulatory Study Approval
Any clinical trial and health related research project which involves humans, their tissues/body fluids and/or data must be reviewed by an independent ethics committee / IRB prior to its initiation.