Our consultants combine not only the
technical expertise in all aspects of web development, data modeling,
configuration management, and systems administration but have the
unique skills and experience in the clinical trials data management
domain. Our consultants combine these skills with the required
project management experience to deliver your project on time and
within budget while meeting the functional requirements of your
project. This means that you are dealing with point-people that are
knowledgeable on all levels and can provide immediate response and
analysis.
Our role is to assist you develop the
right configuration for your trial or study, by working with the data
entry staff to configure an efficient and user-friendly interface,
the bio-statisticians to develop the required data model, and the
principals to meet their overall information management needs within
the technical requirements of the system itself. All this is done in
cooperation with your regulatory and quality assurance personnel to
ensure that your project meets all the necessary compliance.
Experience shows that coordination between your team and our
consultants is key to success.
Our consultants rely on the RDMF.Net
framework for configuration, build, and deployment of your system. It
provides us with the right tools and controls to configure, build, deploy and maintain your system.
