OUR

SERVICES

FROM DESIGN TO PUBLICATIONS

The services range from study design to the development and approval of study protocols, through planning and check points with sponsor, pre-clinical and clinical research (phases 1 to 4), biopharmaceutical development, development of biological assays, monitoring preventive, clinical trial management, data/study management, pharmacovigilance, technical-regulatory support in various approvals, drug dispensing and publications of articles and studies. Science Valley works in an integrated manner in the clinical trial processes that will serve as a basis for the following steps:

1

2

3

4

5

study design, planningand execution

recruitment and follow-up of sampled patients

patenting, registration, manufacturing and marketing

new drugs, molecules, innovative treatments and pharmacovigilance

publication of studies

REMARKABLE EXPERIENCE

Science Valley has experience in the field that gives you confidence in carrying out your research:

 

Os nossos serviços vão do study design ao desenvolvimento e aprovação de protocolos de estudos, passando por planejamento e check points.

HOW WE WORK

To study a drug clinically, it must first be approved in pre-clinical tests, where safety aspects are evaluated in experimental models (animal or cells) before the application of this drug goes to humans. When this medication is ready to be tested in humans, the phases of clinical investigation begin and continue, until the possible volume of contracted information about the medication is obtained. Science Valley is prepared to act in all phases of clinical studies, usually classified into phases: pre-clinical studies and phase 1 to 4 clinical studies. Considering its main objectives and most relevant aspects, each phase of clinical research is summarized as follows:

 

 

WHAT WE DELIVER

With international technical quality standards required and permanently auditable, Science Valley operates with a multidisciplinary team and high medical-scientific capacity, operational technology that follows standards in line with Good Clinical Practices (GCP) and the Brazilian General Personal Data Protection Law. Science Valley is able to test, through its integrated clinical research.

 

 

OUR DIFFERENTIALS