Farmatting
CLINICAL TRIAL AUDIT AND MONITORING SERVICES
Good Clinical Practice (GCP) guaranteed
Our highly trained clinical research associates (CRAs) ensure integrity of study and commitment to excellence—on par with ICH & GCP standards.
Efficient monitoring of clinical sites from site qualification to report generation.
Pubrica offers risk-based high-quality services in clinical trial monitoring to ensure scientific excellence and data integrity across operational centres and regional hubs. Our in-house project management and operations team travel across the globe to support project teams through our local knowledge of the regulatory environment. Our clinical research team members are acquainted with the local laws, regulations and guidelines. We will stand shoulder to shoulder with you on-site—with commitment, passion and motivation to maximize the potential of everyone.
We offer remote monitoring solutions to our customers, which reduce frequency of on-site visits and enhance data quality. Our experts ensure perfect coordination among clinical research associates, project managers, sponsors, and other clinical trial site members.
Pubrica rigorously scrutinizes its CMD services and projects in terms of the teams and resources to ensure details of projects are strictly kept within the operational zone. Through our sophisticated services in CDM, we have transcended the conventional model. We strive to scale new heights in CMD services.
We offer remote monitoring solutions to our customers, which reduce frequency of on-site visits and enhance data quality. Our experts ensure perfect coordination among clinical research associates, project managers, sponsors, and other clinical trial site members.
Pubrica rigorously scrutinizes its CMD services and projects in terms of the teams and resources to ensure details of projects are strictly kept within the operational zone. Through our sophisticated services in CDM, we have transcended the conventional model. We strive to scale new heights in CMD services.
Comprehensive Clinical Trial Monitoring Solutions
- Site selection and feasibility
- Development of recruitment criteria (inclusion and exclusion) with proper consent
- Managing patient recruitment
- Quality assurance mechanisms
- GCP—including training and motivational visits
- Communication with sites
- Customizable training based on the requirements
- Initiation, interim monitoring, and study closure visits
- Managing of local ethics review process
- Study-specific training to site personnel
SCRIPTING SUCCESS STORIES
