What we offer
RALF Monitor, s.r.o. offers the following services:
IN CLINICAL TRIALS:
- Feasibility studies and Investigator site selection
- Creation of documents for local studies : CRFs, patient cards, scales...
- Regulatory document collection and repository
- Regulatory and ethics committee submissions
- Contract preparation
- Training of clinical research personnel
- Study management
- Study site initiating and monitoring
- Study site close-out
- Data management
- Clinical research management in compliance to GCP with all related services
- Quality assurance
IN CLINICAL RESEARCH TRIAL SITE COORDINATION:
- Clinical training for study site personnel / trial site coordinator
- Site management
- Patient Screening and Enrollment
- Schedule follow up visits
- Maintain and dispense drug and other study supplies
- Timely and accurate CRF transcription
- Ensure GCP adherence and compliance
- Data entry and data management as per global regulatory and audit standards
- Prepare site for audit visits and respond quickly to any queries