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- -Protocol feasibility assessment
- -Staff training and certification
- -Standard operating procedure (SOP) development
- -Data management and quality control
- -Targeted patient recruitment strategies
- -Patient screening and enrollment optimization
- -Retention programs and patient engagement tools
- -Patient education and support
- -IRB/EC submissions and approvals
- -Site regulatory document management
- -Audit preparation and support
- -Adherence to GCP and regulatory guidelines
- -Investigator site identification and selection
- -Contract and budget negotiation
- -Investigator meeting coordination
- -Study close-out activities and document archiving
- -High-quality equipment for rent, including [list of equipment]
- -Flexible rental durations to meet your study needs
- -Regular maintenance and calibration to ensure accuracy and reliability
- -Dedicated support for equipment setup and troubleshooting
- -Accredited calibration services for clinical trial equipment
- -Adherence to industry standards and regulations
- -Calibration certificates provided for compliance documentation
- -Calibration scheduling and reminders to ensure equipment accuracy