CRO Sevices
Clinres CRO provides monitoring and study management of:
- clinical trials phase I, II, III, IV
- in all therapeutic areas
- for the original companies and also for the international CROs
- in the Slovak and Czech Republic
We also provide other services associated with clinical trials
- feasibilities, qualified selection of sites, initiation of sites, local investigators meetings
- study start-up activities including preparation of Clinical Trial Applications
- submissions to Regulatory authorities and Multicentric and Local Ethics Committees
- negotiation with institutions and preparing of contracts with hospitals and investigators
- management of safety reporting
- translation of study documents
- training of site stuff for GCP and study specific systems
- every year we have at least one sponsor audit
We also provide other services associated with clinical trials
- feasibilities, qualified selection of sites, initiation of sites, local investigators meetings
- study start-up activities including preparation of Clinical Trial Applications
- submissions to Regulatory authorities and Multicentric and Local Ethics Committees
- negotiation with institutions and preparing of contracts with hospitals and investigators
- management of safety reporting
- translation of study documents
- training of site stuff for GCP and study specific systems
- SOP writing
- every year we have at least one sponsor audit