Epstein Associates assists with Post Marketing Safety Surveillance, regulatory consulting, protocol writing, CRF creation, and research Clinical Development 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.