Global Clinical Research

Overview

Global Clinical Research (GCR) is a full-service Clinical Research Organization (CRO) based in Nepal, providing end-to-end clinical trial solutions to pharmaceutical, biotechnology, and medical device companies worldwide.

Core Services

• Clinical Trial Management: End-to-end support from feasibility studies to final reports, with specialization in Phase III & IV trials
• Regulatory Affairs: Comprehensive regulatory support navigating complex global regulations and securing approvals from NHRC, DDA, and other governing bodies
• Medical Writing: Expert documentation services for protocols, reports, and publications
• Clinical Data Management: Accurate data collection, processing, and analysis across multiple sites with rigorous quality checks and data cleaning
• Patient Recruitment & Retention: Innovative strategies for efficient enrollment and retention throughout clinical trials
• Laboratory Services: State-of-the-art laboratory services supporting clinical trials with accurate and timely analysis
• Clinical Monitoring & Site Management: Regular site visits and comprehensive monitoring to maintain protocol compliance and data quality
• Global Study Coordination: Seamless coordination of multi-center, international clinical trials
• Clinical Logistics: Delivery services for clinical trial materials, samples, and equipment; cold chain management; IP protection

Operational Strengths

• Global reach with local expertise across Nepal and partner CROs beyond
• Highly trained Clinical Research Associates (CRAs) available 24/7 through mobile and online platforms
• Bilingual monitoring capabilities
• Advanced Clinical Trial Management System (CTMS) for real-time data tracking
• ISO 9001:2015 certified
• FDA compliant operations

Therapeutic Focus

GCR conducts trials across multiple therapeutic areas and supports pharmaceutical, biotechnology, and medical device clients.