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;