At AGCR, our unwavering dedication to excellence distinguishes us within the dynamic field of clinical research. We take pride in our distinctive approach and industry-leading practices, solidifying our standing as the partner of choice for organizations navigating the complexities of clinical trials.
Key Differentiators
  • 01. Always-On Client Support
  • 02. Cumulative Professional experience of More than 27 years
  • 03. A meticulously curated network of esteemed investigators, ensuring the highest quality in trial execution through their proven expertise and reliability.
  • 04. Round The Clock Client-centric Service Support (ensuring clients have immediate access to assistance whenever required)
  • 05. Transparent and value-based pricing structures, reflecting a commitment to delivering exceptional value and return on investment for sponsors.
  • 06. Implementation of a robust risk assessment and management framework, proactively identifying and mitigating potential challenges throughout the research process.
  • 07. Adaptable and Customizable Offerings
  • 08. Flexibility and adaptability in tailoring services to meet the unique and evolving requirements of sponsors, ensuring seamless alignment with dynamic study demands.
Quality And Compliance
Elevating Quality Standards through our Robust Quality Management System (QMS)

At AGCR, our commitment to excellence is fortified by a comprehensive Quality Management System (QMS), ensuring compliance with all regulatory and quality standards. Our QMS designates Quality Management as an independent function directly reporting to executive management.
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Comprehensive Quality Policy
Our Quality Policy, approved by executive management, is binding for all staff and collaborators.
Self-regulated Quality Culture
At AGCR, we instill a self-regulated Quality culture, fostering accountability and responsibility among individuals for the integrity of clinical trial data.
Holistic Approach to Quality
We believe that a robust QMS is complemented by an engaged workforce, relevant training, and a culture that encourages innovation and process improvement.
Expertise in Audits
AGCR specializes in various audit types for clinical trials, including Investigator Site Audits, Qualification Audits, Non-Affiliated Audits, Trial Master File (TMF) Audits, Phase I site Audits, For Cause Audits, System Audits, Vendor Audits, and Data Audits.
Quality Oversight Mechanisms
  • Internal and External Audit Programs
  • Multi-level approval for Quality documents
  • 21 CFR Part 11 compliance for all systems
  • Formal Corrective and Preventive Action (CAPA) process
  • Six Sigma and Lean methodologies for process optimization
  • Business Continuity Program (BCP) and Disaster Recovery (DR)
  • Continuous ICH GCP audits and training programs
  • Industry-leading 21 CFR Part 11 compliant QMS software utilization for seamless SOP approval, training, documentation, CAPA, and audits.
Experience the pinnacle of quality in clinical research with AGCR's unwavering commitment to excellence.
Innovation And Technology
We are dedicated to incorporating innovative approaches and harnessing state-of-the-art technologies to optimize the efficiency and effectiveness of our clinical research processes.
We proactively integrate the following advancements:
Electronic Data Capture (EDC) Systems
We utilize advanced electronic data capture systems that enable secure and streamlined data collection, management, and analysis. EDC systems replace traditional paper-based methods, allowing for real-time data entry, automated validation checks, and efficient data cleaning processes. This accelerates data availability, minimizes errors, and enhances overall data quality.
Remote/Central Monitoring Capabilities
We harness the power of remote/central monitoring technologies to facilitate real-time oversight of clinical trials. Remote/Central monitoring allows for continuous monitoring of study activities, data collection, and protocol compliance from a distance. By utilizing secure platforms and electronic communication, we can promptly identify and address any potential issues, ensuring study integrity and participant safety.
Real-time Data Analytics
We employ advanced data analytics tools and techniques to perform real-time analysis of collected data. By leveraging these capabilities, we can generate valuable insights, identify trends, and make informed decisions during the course of the study. Real-time data analytics empower us to proactively adjust study protocols, optimize recruitment strategies, and ensure timely decision-making.
By incorporating these innovative approaches and technologies into our clinical research processes, Akshar Global Clinical Research strives to optimize efficiency, enhance data quality, and improve the overall participant experience.