Centre of Excellence Clinical Research

ABOUT

Centre Of Excellence Clinical Research

The Center of Excellence for Clinical Research (CECR) is envisioned to be a premier institution dedicated to advancing medical knowledge and improving patient care through high-quality clinical research. This comprehensive booklet serves as a guide for establishing such a centre, providing detailed information on its vision, mission, organizational structure, and services. By adhering to the guidelines within, you can develop a robust and efficient research centre that meets the highest standards of excellence. The CECR aims to bridge the gap between scientific discoveries and clinical application, ultimately benefiting patients and healthcare providers alike. With a focus on collaboration, innovation, and ethical conduct, the centre is poised to make significant contributions to the field of clinical research. This document outlines the necessary steps and considerations to ensure the successful launch and operation of the CECR.

Dr. Rajanikanth Vangala
Director Clinical Research

Dr. Rajanikanth Vangala is the Director of the Centre of Excellence in Clinical Research at InARI. With over 25 years of experience in clinical trials and research methodologies, Dr. Vangala has been pivotal in advancing clinical research initiatives. His expertise and dedication ensure that InARI remains at the forefront of innovative clinical solutions and patient care advancements.

FOCUS

Focus Areas

Pharma
In Vitro Diagnostics
Medical Devices

Our Vision and Mission

Our vision is to become a global leader in clinical research, recognized for our excellence, innovation, and significant impact on healthcare. We are driven by our mission to innovate through groundbreaking research, develop novel treatments and therapies, and collaborate with leading academic institutions, industry experts, and healthcare providers. By educating and training the next generation of clinical researchers, we aim to ensure the future of high-quality clinical research. Our commitment to improving patient care and outcomes through the translation of research findings into clinical practice is at the core of our mission. We strive to maintain the highest ethical standards in all our research activities, ensuring transparency, accountability, and respect for all participants. Through these efforts, we aim to make meaningful contributions to the advancement of medical science and patient health.

State-of-art Infrastructure

🧬 Expert teams specializing in the design and development of clinical trial protocols.

🧬 Collaboration with key stakeholders to ensure protocols are scientifically sound and feasible.

🧬 Comprehensive support for obtaining Ethics Committee (IRB) approval.

🧬 Assistance with preparing and submitting all required documentation to ensure ethical compliance.

🧬 Advanced tools and methodologies for identifying and selecting optimal trial sites.

🧬 Detailed feasibility assessments to ensure site capabilities match trial requirements.

🧬 Dedicated Clinical Research Units (CRUs) for managing and conducting clinical trials.

🧬 Coordination of trial activities, including patient recruitment, enrollment, and follow-up.

🧬 Expertise in navigating complex regulatory landscapes across multiple jurisdictions.

🧬 Support for regulatory submissions, approvals, and ongoing compliance with global standards.

🧬 Secure data management systems for efficient trial data collection, storage, and analysis.

🧬 Advanced biostatistical services to ensure accurate interpretation and reporting of study results.

🧬 On-site and remote monitoring to ensure compliance with Good Clinical Practice (GCP) guidelines.

🧬 Quality assurance programs to maintain high standards of trial conduct and data integrity

🧬 Facilities designed to foster collaboration with pharmaceutical companies, biotech firms, and academic institutions.

🧬 Support for joint research initiatives and multi-center studies.