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Performance Catalogue
Monitoring clinical studies of phase 1 – 4 in all indications:
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- Selection and approval of sites
- Initiation of clinical studies, training and development of site staff
- Obtaining documents and creation of worksheets
- Communication between sponsor and site
- On-site monitoring: eligibility, safety, source data verification, query management, service and support of site staff
- Control of study medication and material: receipt, storage, usage, accountability, transfer, destruction
- Payment, establishment and actualization of tracking lists
- Closing and rating of study sites
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As a further service I am offering:
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- Training and development of foreign staff members
- Adjustment of Monitors to transfer of studies and sites
- Co-monitoring
- Agency of freelanced CRA`s
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