Epstein Associates assists with Post Marketing Safety
Surveillance, regulatory consulting, protocol writing,
CRF creation, and research study design.  Dedicated
professionals with experience in monitoring initial
adverse event data intake, response to medical
inquiries and product complaints assist in your
clinical research pathway. Epstein Associates will
provide active query and case data entry into client
pharmacovigilance systems.  Preparation of MedWatch,
CIOMs and periodic reports for submission to
regulatory agencies, comprehensive literature review
as well as analysis and medical review are also
available to our clients.