Clinical Research Automation
Digital solutions for tracking study timelines and regulatory applications
Pharmaceutical Research Process Automation
At Nobel İlaç, I led the development of digital solutions to streamline clinical research workflows and improve efficiency in regulatory processes.
Key Accomplishments
- Developed an online platform that integrates IMP (Investigational Medicinal Product) procurement with regulatory affairs requests, creating a centralized system for better coordination
- Built RPA (Robotic Process Automation) software in collaboration with a vendor to track study timelines for clinical trials and bioequivalence studies
- Implemented automated tracking for Ethics Committee (EC) and Ministry of Health (MoH) applications, reducing manual monitoring effort and providing real-time status updates
- Improved overall process efficiency and reduced administrative burden through strategic automation of repetitive tasks
- Enhanced data visibility across departments by creating centralized dashboards for clinical study status monitoring
Impact
These automation initiatives significantly improved process efficiency, reduced manual workload, and provided better visibility into study timelines across the organization. The system enables more accurate forecasting and planning for clinical studies, resulting in better resource allocation and regulatory compliance.
Technologies Used
- RPA (Robotic Process Automation)
- Web-based platforms for data integration
- Process workflow optimization
- Regulatory compliance tracking systems