• 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 » Spaulding Clinical partners with clinicalRSVP

Spaulding Clinical partners with clinicalRSVP

March 14, 2012
CenterWatch Staff

West Bend, Wisc.-based Spaulding Clinical Research is partnering with clinicalRSVP (clinical Research Subject Verification Program), a provider of participant registry services in North America.

Spaulding Clinical is joining participating clinical sites that utilize clinicalRSVP to check participant eligibility requirements before dosing commences. Spaulding Clinical is the first site in the Midwest to join clinicalRSVP’s network, which includes sites on both coasts.

Spaulding Clinical said it chose clinicalRSVP as its preferred provider of dual enrollment protection services because of its expansive network, proven track record, ease of operational implementation and regulatory compliance. clinicalRSVP has developed a network of sites that currently includes more than 25% of all phase I beds in North America.

“Dual enrollment is becoming an incredibly hot topic in the clinical pharmacology circuit as sponsors are becoming very keen to ensure subjects are only in their studies,” said Daniel Selness, general manager and senior vice president of operations at Spaulding Clinical. “Spaulding is pleased to be able to provide this added measure of diligence for our study sponsors.”

“The addition of Spaulding Clinical represents a terrific advancement for clinicalRSVP and for those who sponsor and conduct phase I clinical trials across North America,” said Darran Boyer, president of clinicalRSVP. “We are pleased that our network now spans from coast to coast, including the Midwest and into Canada.”

clinicalRSVP is a North American network that prevents research volunteers from enrolling in multiple research studies concurrently. This blinded cooperative registry allows investigators to confidentially and securely verify patient eligibility requirements prior to patient enrollment in clinical trials, resulting in advances to clinical research data integrity and participant safety.

Spaulding Clinical Research provides clinical pharmacology and cardiac core lab clinical research services, and is a medical device manufacturer. It operates a 105-bed clinical pharmacology unit with 96 beds of telemetry. As a phase I-IV core ECG laboratory provider, Spaulding Clinical offers equipment provisioning and electrocardiograph over-reading services.

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