provides a wide range of services for the review and oversight
of clinical studies. Our customers are pharmaceutical and device
manufacturers (sponsors) and the contract research and site management
organizations that serve them. We also serve institution and physician-sponsors.
list of services. Or, perhaps we can design a custom program to
fit your unique requirements.
Initial and ongoing review of clinical research protocols and
investigative sites (including the informed consent process and
On-line IRB study document submission tracking
Delivery of IRB research review documentation within 48-hours of the
Good Clinical Practice (GCP) audits and training.
On-site evaluation of the informed consent process.
Informed consent writing, templates & translations.
Statistical support for de-identification of protected health
at 877-793-8900 to discuss your needs.