GraySail offers a number of services for Universities, Hospitals, or Clinical Research Centers with special research management needs, including assessment, workflow implementation, and technology development and implementation.
Human
Subjects
Clinical research managers face constant
challenges to design and implement consistent processes to protect the human
subjects of clinical trials. In recent years, a number of high-profile failures
in these practices have led to heightened scrutiny by federal regulators.
GraySail understands the special needs of clinical research managers and can
help you implement an open and auditable process that enhance the safety of
human subjects and minimizes the risk exposure of critical clinical trial
programs.
Institutional Review
Boards
GraySail is familiar with the document
management and distribution needs of IRBs. We use that experience to develop
workflows that leverage existing data stores with secure intranet technology…
making sure that accurate information is delivered to the right reviewer in
electronic form, and eliminating accidental circumvention of procedure. And
because GraySail uses standard tools to develop a custom solution that draws on
your existing data repositories, our solutions preserve your existing data and
reduce start-up costs.
Professional
Oversight
Good research managers are not looking for a
nifty technology solution. They're looking for a way to leverage technology to
make sure their research programs are ethical, well-documented, and audit-ready.
That's why we work closely with each client's research compliance officers or
consultants to make sure that the solutions we help implement are not only
highly usable, but also fully compatible with existing and emerging compliance
programs.
