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