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Pharmaceutical

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.

Key Services

  • Clinical & Medical Consulting
  • Business Development
  • Pharmaceutical
  • Regulatory Affairs
  • Legal Consulting

News & Announcements

Achieving successful bowel preparation with evening/morning split-dosing regimens of NER1006 versus trisulfate: post hoc analysis of a Phase 3 trial
Jul 25, 2017
Novel 1L Polyethylene Glycol (PEG)-Based Bowel Preparation NER1006 Achieves High Quality Bowel Cleansing with a Lower Volume than Standard 2L PEG + Ascorbate and Under 3L Total Fluid Volume Intake
Jul 25, 2017
Bowel preparation quality of NER1006 versus oral trisulfate solution as assessed by colonoscopists at site: a post hoc analysis from a randomized controlled trial
Jul 25, 2017

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Epstein Associates, LLC
621 Ridgely Avenue, Suite 204
Annapolis, MD 21401

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