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GIGA MEDICAL is European contract research organization (CRO) doing
Clinical Research, Safety Surveillance, Regulatory Affairs, Clinical Trials, and Medical Affairs
related to development of new medical compounds that enables pharmaceutical and biotechnology companies implement their products to worldwide markets.
GIGA MEDICAL assists investigators in planning, conducting, and reporting clinical trials.
GIGA MEDICAL is organizing, coordinating, controlling, conducting, and administering clinical trials and researches.
Our CRO services include:
- Clinical project management
- Monitoring of phase I-IV studies
- Regulatory affairs
- Clinical development plans
- Data management
- Training
- GCP and regulatory training
- Conduct and monitoring of clinical trials (all phases and indications)
- Consultancy in regulatory environment
- Meeting planning and event management
- Quality of Life Projects: translation, pilot testing, proofreading
Our employees are all trained according to the guidelines for Good Clinical Practice (GCP). These guidelines are the basis of our company's standard operating procedures (SOPs). Our employees are also certified compliant to Adverse Drug Events – Reporting & Regulatory requirements by Center for Professional Innovation and Education (CfPIE).
We are highly competitive in quality, time and cost - particularly as we can provide clients with reliable and consistent feasibility information before the costly drug development.
