G&G Medical Technology is Contract Research Organization specialized in observational studies and post-approval research: Phases III and IV clinical trials, post-market surveillance. It is registered with the OsSC (National Monitoring Centre of Clinical Trials of Drugs) according to Ministry of Health Decree dated the 31of March 2008 and it is also certified ISO 9001:2008 by Bureau Veritas
Our CRO works according to Standard Operating Procedures (of its own as well as of its clients) and in line with the standards for good clinical practice (ICH-GCP).
Our CRAs have long experience in monitoring international studies and communicating with Ethics Committees and local regulatory authorities.
- Clinical Trial design
- Protocol and CRF design
- e- CRF design
- Trial planning and budgeting
- Site negotiation
- Ethic and administrative activation
- On site monitoring
- Project management
- Data management and statistics
- Analysis and reporting
- Medical Writing
- Investigators’ meeting