Contract Research Organization
Clinical Trial Management
We help plan, initiate, manage, and monitor clinical trials for pharmaceutical and biotechnology companies. This includes Phase I-IV clinical trials.
Regulatory Affairs
We assist in navigating complex regulatory requirements and obtaining approvals from regulatory authorities for clinical trials and drug approvals.
Clinical Data Management
We handle data collection, validation, analysis, and reporting of clinical trial data, ensuring data quality and compliance with regulations.
Biostatistics and Data Analysis
We provide statistical analysis and reporting of clinical trial results to support decision-making and regulatory submissions.
Clinical Site Selection
We help sponsors identify and select appropriate research sites for clinical trials, considering factors like patient populations, geography, and expertise.
Project Management
We manage the entire clinical trial process, ensuring it stays on track, on budget, and within regulatory compliance.
Monitoring and Site Management
We oversee the activities at clinical trial sites, ensuring protocol adherence, patient recruitment, and data quality.
Clinical Supplies Management
We handle the logistics of clinical supplies, including drug distribution, labeling, and inventory management.
Quality Assurance and Auditing
We ensure trials adhere to Good Clinical Practice (GCP) and regulatory standards through auditing and quality control.
Patient Recruitment and Retention
We develop strategies to attract and retain trial participants, crucial for the success of clinical trials.
Management of printing
We offer a printing service of Investigators Site Files and any other study related documents.