About Us

CDMC provides a wide range of services in the data management area and serves the pharmaceutical & biomedical industry throughout all types and phases of clinical trials. The Company utilizes state of the art technologies combined with decades of practical experience to offer a complete range of clinical data management, biostatistics, data analysis and reporting solutions, from early planning to reporting and published results.
We offer client-specific solutions to the various sectors of the life science industry. Our services are based on extensive know-how and vast familiarity with the biomedical community. We understand from within our customers’ business, the challenges they face and the high standards needed to ensure their success. It enables us to provide high quality and cost-effective solutions.

CDMC provides you with advanced data management, analysis and reporting solutions alongside the assurance of quality and precision.

CDMC is a Bioforum Professional company – the professional services arm of Bioforum Applied Knowledge Center.

In any clinical trial, all data must be maintained in top-notch quality and be available in real-time for internal trial management processes as well as regulatory submissions, publications and periodic safety update reports.

From expert consultation, through design of key elements of your trial to full turn-key project outsourcing – CDMC meets all of your data management, analysis and reporting needs. We support both paper data entry and Electronic Data Capture (EDC) systems, utilizing Clintrial™, Oracle Clinical, InForm™ and Oracle RDC as needed. We use GCDMP (Good Clinical Data Management Practice), the industry standard for clinical data management, as a guide for performing our services, all of which are also fully compliant with GCP, ISO 14155 and other international and local regulatory standards.

The company’s management team consists of experienced data management personal who can provide customized, high-quality, comprehensive services that meet the study design, specific client requirements and budget in a timely, cost-effective manner.

Faster access to reliable and of high quality clinical trial data can improve decision making and accelerate overall clinical development. Professional clinical data management will increase the company’s value and will shorten the time to receiving the desired approvals from regulatory agencies.