• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trials
    • Search Clinical Trials
    • Patient Notification System
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Clinical Trial Listings
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • JobWatch
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Trial Listings
  • Advertise
  • COVID-19
  • iConnect
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » ClinicalRM, Ohio Clinical Trials Collaborative partner

ClinicalRM, Ohio Clinical Trials Collaborative partner

June 25, 2014
CenterWatch Staff

CRO ClinicalRM and the Ohio Clinical Trials Collaborative (OCTC) have announced a co-marketing partnership offering joint services for clinical trials of new biologics, drugs and medical devices. The relationship will serve the organizations’ mutual customers with a full spectrum of development services including access to a network of veteran investigators, patient population identification, clinical operations and guidance on medical/regulatory affairs.

“Expedited access to Ohio’s premier medical institutions will shorten the time to start a new multi-site clinical trial, as well as assure timely patient enrollment for our clients,” said Alan Braverman, Pharm.D., vice president of clinical operations of ClinicalRM, a 20-year-old, full-service CRO headquartered in Ohio. The firm has over 350 employees.

The OCTC offers centralized access to Ohio’s premier medical centers for trial development. It is a statewide initiative that streamlines contracting, budgeting, approval of human subject use and patient recruitment/enrollment processes to move medical discoveries to market faster. ClinicalRM supports these clinical trials with an array of clinical operations, quality management and regulatory affairs services, along with a regional and globally experienced scientific advisory board.

“Integrating ClinicalRM’s services into the OCTC’s clinical trials network will provide a powerful engine for new pharmaceutical, biologic and medical device development in Ohio,” said John Peterson, Ph.D., global business development director of the OCTC.

Upcoming Events

  • 24May

    Powering an Effective Oversight Strategy with Clinical and Operational Insights

  • 25May

    2022 WCG Avoca Quality & Innovation Summit: Own the Future

  • 28Jun

    Effective Root Cause Analysis and CAPA Investigations for the Life Sciences

  • 16Oct

    WCG MAGI's Clinical Research Hybrid Conference - 2022 West

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

  • Protocol-360x240.png

    Avoid Deviations by Making Protocol Review a Team Effort

  • SelectionProcess-360x240.png

    Give Us a Voice: Sites Clamor for a Say on Vendor Selection

  • Convince-360x240.png

    Use Data and Details to Convince Site Leadership to Add Staff

  • AsktheExpertsBadge-360x240.png

    Ask the Experts: Listing Trial Staff and Others on the Statement of Investigator

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 My Personal Information

Footer Logo

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

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2022. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing