Investigator Initiated Studies (IIS) are studies where an individual investigator, a research site, or a group of research sites carry out the research from the protocol design until regulatory submission. This means they perform both roles, as a sponsor and as an investigator.
Each day countries and institutions look to increase their scientific capability to deliver new and modern drug options for patients, new therapeutics indications for already licensed drugs, cost-effective evaluations, and new drug pharmaceutics ways.
Investigator Initiated Studies (IIS) are an excellent opportunity for investigators to fund totally of partially their studies with private pharmaceuticals or government grants. These programs include study methods such as interventional, observational, and Real World Evidence (RWE).
The strategic alliance between VaxTrials, a renowned Latin American CRO, and Integra IT, a company expert in software development for clinical studies, aims to maximize the capabilities of researchers and accompany them throughout the process from the application to IIS programs in the industry to the cost-effective execution of the study. Including services from the construction of the brief with the hypothesis or research idea to the operational conduct and data management of the clinical study.
Medical Writing services Include:
The project management service includes:
Data management services include:
Biostatistics services include:
Clinical Trial Management Software:
Investigator-Initiated Studies (IIS) are studies where an individual investigator, a research site, or a group of research sites carry out the research from the protocol
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