Because you don’t need just a solution, but rather the most integral and suited solution, our services constitute the best option to support you during the development of your program.
Our main services are:
- Feasibility Studies
- Consulting and assistance for the complete design of clinical research documents in compliance with International Good Clinical Practices (GCP’s), and Standard Operation Procedures (SOP’s)
- Project Planning
- Clinical Plan Development
- Site Identification and Assessment
- Regulatory Affairs
- Coordination of Investigational Sites
- Clinical Monitoring
- Medical Monitoring
- Quality Assurance
- Management of drug and laboratory samples
- Registration of new products / indications
