Comprehensive management of clinical trials and healthcare services to ensure
safety, efficiency, and regulatory compliance throughout the lifecycle of your
clinical research project from start to finish.
Projects Delivered
Accelerate Audits
Trial Completion Rate
Participants Engaged
Global Clinical Research (GCR) manages the archival of records and documents from both internal and external sources, including research sites, ensuring compliance with sponsor requirements for both short- and long-term storage. Our archival processes covering maintenance, disposition, disaster prevention, and record recovery adhere strictly to GCR's Standard Operating Procedures (SOPs).
Comprehensive protocol development, site selection, and participant management for successful trials.
Expert oversight ensuring adherence to GCP guidelines, patient safety, and data integrity.
Advanced software solutions and vendor integration for streamlined trial operations.
Clinical Trial Planning & Site Management
Development of comprehensive study protocols tailored to specific trial objectives and research goals.
Implementing effective strategies to ensure participant adherence to trial protocols and regulatory standards.
Identifying appropriate trial sites, training site staff, and overseeing site operations to ensure protocol adherence.
Preparation and submission of trial documents in compliance with Good Clinical Practice (GCP) and international guidelines.
Collection, analysis, and monitoring of safety data to meet regulatory reporting requirements and ensure participant wellbeing.
Expert oversight to ensure patient safety and scientific integrity, including review of patient data, adverse events, and protocol deviations.
Regulatory Compliance & Safety Monitoring
Technology & Data Management
Using Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS) to streamline data collection, patient tracking, and trial monitoring.
Implementing robust data security measures to protect sensitive patient information and ensure compliance with data protection regulations.
Collaborating with Contract Research Organizations (CROs) for monitoring, data management, and patient recruitment to enhance trial efficiency.
Our experienced team delivers exceptional clinical operations services with a
focus on quality, efficiency, and compliance.
We streamline processes to save time and reduce costs.
Ensuring all trials meet global standards and regulations.
Ethical trial management with strict monitoring and data integrity.
We follow a systematic methodology to ensure successful clinical trial execution from planning to completion.
Comprehensive evaluation of research objectives, protocol development, and resource planning.
Identifying optimal research sites, training staff, and establishing operational procedures.
Implementing the protocol with rigorous oversight to ensure compliance and data quality.
Collecting, processing, and analyzing trial data with advanced technological solutions.
Comprehensive documentation, regulatory submissions, and proper trial conclusion procedures.
