Comprehensive Solutions

Other Clinical Services

GCR is a full-service Clinical Research Organization (CRO) and biopharmaceutical service provider supporting pharmaceutical, biotechnology, and medical device companies. With innovative technologies and therapeutic expertise, we help clients accelerate the delivery of safe and effective treatments while maximizing R&D success.

Our Expertise

At GCR, we combine expertise, technology, and commitment to quality to drive successful clinical trials.

End-to-End Clinical Trial Support

From feasibility studies to final reports, specializing in Phase III & IV trials.

Global Reach, Local Expertise

Strong collaboration with site staff and partner CROs across Nepal and beyond.

Expert Monitoring & Oversight

Our highly trained Clinical Research Associates (CRAs) proactively manage trials to ensure accuracy, compliance, and efficiency.

Always Connected

Our bilingual monitors are available 24/7 through mobile and online platforms.

Our Clinical Services

We provide a comprehensive range of clinical services tailored to meet the unique needs of each client and research project.

Tailored Clinical Research Solutions

Customized research approaches designed to meet specific client objectives and requirements.

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Study Document Development

Creation of comprehensive protocols, case report forms, and other essential study documents.

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CRA Management & Quality Control

Oversight and training of Clinical Research Associates to ensure consistent quality standards..

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Clinical Monitoring & Site Management

Regular site visits and comprehensive monitoring to maintain protocol compliance and data quality.

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Clinical Trial Management System (CTMS)

Advanced software solutions for efficient trial management and real-time data tracking.

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Investigator Meeting Planning

Organization and facilitation of productive investigator meetings to align study objectives.

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Third-Party Vendor Management

Coordination with external vendors to ensure seamless integration of services and deliverables.

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Audits & Compliance Preparation

Comprehensive preparation for regulatory inspections and sponsor audits to ensure readiness.

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Training & Development

Educational programs for research staff to enhance skills and maintain regulatory compliance.

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Patient Recruitment & Retention

Strategic approaches to identify, enroll, and retain appropriate study participants.

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Feasibility Studies

Thorough assessment of study viability, site capabilities, and participant availability.

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Quality Training for Clinical Associates

Specialized training programs to ensure all research associates maintain the highest standards.

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Looking Forward

Future Plans

GCR is dedicated to advancing healthcare by generating evidence-based results in the fields of clinical and public health research. We plan to support national planning with actionable, evidence-based insights and contribute to the global scientific community by conducting and publishing high-impact journals.

Expanding our research capabilities to address emerging healthcare challenges

Strengthening international partnerships to facilitate global research collaboration

Investing in advanced technologies to enhance research efficiency and data quality

Future of Clinical Research

Elevate Your Clinical Operations

Collaborate with us to streamline your clinical trial processes, ensuring efficiency, compliance, and success on a global scale.