• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trial Listings
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Directories » Useful Resources » PMG Research, Inc.

AND
  • A
  • B
  • C
  • D
  • E
  • F
  • G
  • H
  • I
  • J
  • K
  • L
  • M
  • N
  • O
  • P
  • R
  • S
  • T
  • U
  • V
  • W
  • Z

PMG Research, Inc.

  • Profile

Profile

PMG Research, Inc.

Contact Information

Contact: Kathy Cole
Phone: 919.746.7106
Email: Click here to see email.
Website: http://www.pmg-research.com

Center Information

Kathy Cole
Director of Feasibility
PMG Research, Inc.
4505 Country Club Road, Suite 110
Winston-Salem, NC 27104
919-746-7106
kcole@pmg-research.com
www.pmg-research.com

Currently Enrolling Trials

    Show More

    Company Overview

    PMG Research, Inc. is an Integrated Site Network (ISN) of fourteen clinical research facilities in the United States. Since its founding in 1979, PMG has conducted over 8,100 research studies for hundreds of pharmaceutical sponsors and CROs. At PMG Research, Inc. our mission is to bring clinical research to as many lives as possible while delivering unparalleled service and exceptional value to our clinical trial partners and stakeholders.PMG Research is a fully-integrated network of sites employing 200 highly-trained clinical research professionals across 14 hub cities throughout Illinois, Iowa, North Carolina, South Carolina and Tennessee. Our patient-centric organization ensures consistency, compliance, and the highest quality performance and results on a trial.

    • Research staff received national ranking, recognized as Top U.S. Researchers in 2012, 2013, 2015, 2018
    • 150+ Physician Investigators and 100+ Clinical Research Coordinators spanning 53 practice affiliations
    • Over 8,100 completed Phase I - IV studies; experience across all therapeutic areas and device trials
    • Above industry average start-up, patient retention, and patient satisfaction rates
    • Master Service Agreements and strategic partnerships with select Sponsor, CRO, and healthcare organizations

    The Value of PMG Research

    • Contractual relationships with large, multi-specialty physician practices and healthcare institutions providing Electronic Medical Record (EMR) access to nearly 3 million active patient lives
    • Proprietary database of over 280,000 engaged past or potential research participants
    • Centralized data-driven feasibility process, including participant pre-identification via EMR
    • Internal project management services for multi-site and network-wide trials provides ease of contracting and a single point of accountability throughout the trial
    • Training & compliance team ensures we are always audit-ready
    • Standardized SOPs and premier training program allow cross-utilization of research staff and physician collaboration
    • Dedicated patient engagement & recruitment team implements fully-integrated recruitment and retention campaigns
      • Physician practice outreach
      • Community outreach and public relations
      • Email/direct mail database and external outreach
      • Digital, social, and traditional media marketing

    Quality Data

    • Premier training program and internal QA staff.
    • Integrated SOPs developed to ensure compliance with GCPs, subject safety and data integrity.
    • Web-based CTMS includes patient volunteer, sponsor and study database.
    • Central IRBs.
    • Regulatory document turnaround of 3 business days on average.
    • Contract finalization of 10 business days or less.
    • Master Clinical Trial agreements.
    • TempGuard devices for continuous temperature monitoring of investigational drug.

    Staff & Investigator Experience

    • Collectively, PMG sites have 100 years of experience conducting Phase I-IV clinical trials
    • 200 research staff averaging over 5 years of experience
    • 150 experienced Principal Investigators averaging over 10 years of research experience
    • 100 Clinical Research Coordinators averaging 5 years of experience

    Our Integrated Network

    PMG Research of Bristol CenterWatch | PMG
    PMG Research of Cary CenterWatch | PMG
    PMG Research of Salisbury CenterWatch | PMG
    PMG Research of Charlotte CenterWatch | PMG
    PMG Research of Charleston CenterWatch | PMG
    PMG Research of DuPage Medical Group CenterWatch | PMG
    PMG Research of McFarland Clinic CenterWatch | PMG
    PMG Research of Piedmont HealthCare CenterWatch | PMG
    PMG Research of Winston-Salem CenterWatch | PMG
    PMG Research of Raleigh CenterWatch | PMG
    PMG Research of Rocky Mount CenterWatch | PMG
    PMG Research of Hickory CenterWatch | PMG
    PMGResearch of Wilmington CenterWatch | PMG
    PMG Research of Knoxville CenterWatch | PMG

    Back to Listings

    Upcoming Events

    • 25Apr

      Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials

    • 26Apr

      FDA’s New Laws and Regulations: What Drug and Biologics Manufacturers Need to Know

    • 27Apr

      Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis

    • 17May

      2023 WCG Avoca Quality Consortium Summit

    • 21May

      WCG MAGI Clinical Research Conference – 2023 East

    Featured Products

    • Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

      Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

    • Surviving an FDA GCP Inspection

      Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

    Featured Stories

    • tablet

      Digital Intake Platforms Effective as Source of Trial Information, Survey Shows

    • Diversity-360x240.png

      Site Spotlight: EmVenio Research Takes to the Road to Promote Trial Diversity

    • Five Ws

      Consider the Five ‘W’s to Understand Potential Participants

    • QandA-360x240.png

      Perspectives from Smaller-Sized CROs: Q&A with Cheryle Evans

    Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

    The information you need to adapt your monitoring plan to changing times.

    Learn More Here
    • About Us
    • Contact Us
    • Privacy Policy
    • Do Not Sell or Share My Data

    Footer Logo

    300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

    Phone 617.948.5100 – Toll free 866.219.3440

    Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing