Promedica plans to participate in the following industry conferences and trade association meetings. We welcome you to stop by and learn more about us.

OIS@ASCRS – Los Angeles, CA  May 4, 2017

ASCRS – Los Angeles, CA  May 5-8, 2017

ARVO – Baltimore, MD  May 7-11, 2017

Outsourcing in Clinical Trials East Coast – King of Prussia, PA  May 23-24, 2017

Outsourcing in Clinical Trials New England – Boston, MA  September 6-7, 2017

RAPS – National Harbor, MD  September 9-12, 2017

OIS@AAO – New Orleans, LA  November 9, 2017

AAO – New Orleans, LA  November 11-13, 2017


Because our staff and consultants are considered thought leaders in the CRO industry, we are often tapped for our knowledge by both industry/trade publications and conferences. Below are a few examples:

August 2012 Regulatory Affairs Certification Study Group GCP Overview

January 2010 Medical Device and Pharmaceutical Development Overview Training Video

3rd Frontiers in Biomedical Devices Conference & Exhibition, June 2008
Strategies for Clinical Studies & Human Factors Research

Regulatory Affairs Certification Discussion Group, September 2008
Good Clinical Practice
Good Laboratory Practice CFR 21 Part 58
Investigational Device Exemptions 21 CFR Part 812
Investigational New Drug Application 21 CFR Part 312

more (click to access)

Marketing Brochures/Ads

Things to Consider When Selecting a CRO
PMI Ophthalmology Capabilities
PMI - Who We Are
CRO Services for Aesthetics Clinical Research
CRO Services for Medical Device Clinical Research
What Sponsors Say About Working With PMI
Case Studies From PMI
Class III Ophthalmic Device: Pivotal Study. Aggressive Timeline.
Case Studies From PMI
New Compound Indication: Strategic Assessment of Clinical Study Feasibility
Case Studies From PMI
Class III Device: Acquisition and Adjudication