Our professionals have experience in various therapeutic areas, including Oncology, Rheumatology, Vaccines, Gynecology, Ophthalmology, Cardiology, Pulmonology, Diabetes, among others.

With a dynamic structure, we are able to meet your project needs, regardless its size and complexity.

Conducting and coordinating clinical studies (phase II and III) :

  • Preparation and analysis of clinical trial budgets;
  • Selection of researchers and technical staff;
  • Organization and submission of regulatory documents to the competent authorities (CEP-CONEP);
  • Biological material processing and logistics;
  • Receipt, storage and dispensing of products under investigation;
  • Recruitment and selection of research subjects;
  • Data collection and filling of medical records;
  • Administrative support to clinical research centers;
  • Advice and contract management in clinical research;