Our experienced team provides end-to-end management of clinical trials, from initial design through to data analysis and reporting. We offer:
Study Design & Protocol Development
Collaborate with you to design robust, scientifically sound study protocols tailored to your specific research objectives.
Regulatory Affairs & Compliance
Navigate the complex regulatory landscape to ensure all aspects of your trial meet ethical and legal standards.
Site Selection & Management
Identify and manage high-quality clinical sites to ensure your trial is conducted efficiently and effectively.
Patient Recruitment & Retention
Develop and execute strategies to recruit and retain participants, ensuring diverse and representative patient populations for your study.
Data Collection & Analysis
Implement rigorous data collection methods and provide comprehensive statistical analysis to ensure the integrity and validity of your trial results.
Medical Writing & Reporting
Prepare high-quality study reports, publications, and regulatory submissions that clearly communicate your research findings.
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INSTITUTE OF BIOLOGICAL, BIOCHEMICAL & PHARMACEUTICAL SCIENCES (IBBPS)