Clinical Services - Pharmaceutical Regulatory Consulting | GRP

Committed to your success, from Concept to Approval.

Clinical Services - Pharmaceutical Products Regulatory Consulting

Upcoming Events

  1. Drug Development Forum

    September 25 - September 27
  2. BioJapan-2017

    October 11 @ 8:00 am - October 13 @ 5:00 pm
  3. Bio International Convention 2018

    June 4, 2018 - June 7, 2018
  4. Biotech Japan

    June 27, 2018 - June 28, 2018

GRP provides Regulatory, Clinical and Compliance services across the globe

North America
Latin America
Asia
European Union
Australia

Choose the Country

Learn more about how we can assist you with Regulatory, Clinical and Compliance services in your country of interest

PHARMACEUTICAL PRODUCTS CONSULTING

Clinical Services

Our professionals apply their therapeutic, regulatory, and operational expertise to consistently make sure that your clinical studies are conducted with ICH guidelines and other applicable regulatory requirements.

In an increasingly challenging environment, we have the experience and knowledge to find, recruit, and retain patients in clinical trials. We successfully deliver access to appropriate sites and patients, developing strategies that will minimize the risks inherent in patient recruitment.

Our clinical service for national and/or international multi-site trials includes:
  • Protocol development
  • Site and investigator identification and qualification
  • Site initiation and training
  • Clinical monitoring
  • Medical monitoring
  • DSMB coordination
  • Statistical analysis
  • Electronic data capture
  • Electronic Trial Master File
  • Full service data management
  • ClinicalTrials.gov registration and management
  • Central lab oversight and coordination
  • Site quality assurance audits
  • Integrated final Clinical Study Report

Contact us today to learn more about how we can assist your company with clinical services.