OUR COMPANY
Thera Research provides clinical trial services for medical research studies in all diseases, offering flexibility in response to our clients outsourcing demands. Thera Research assists you throughout the clinical trial processes, including but not restricted to: Site identification, strategic feasibility, site selection, strategic site partnerships, investigator qualifications, activation (local regulatory submissions, site contracting and clinical startup), patient recruitment follow up and site closure.
Thera Research ltd. has a vast experience in facilitating the Regulatory process through our Technical Director that interacts with the Local Regulatory Authority “ISP” (Instituto de Salud Pública) for importing the Investigational Medicinal Product (IMP).
Our deep understanding of clinical trial management enables us to minimize study timelines, which can critically impact on the success of the study.
CLINICAL TRIAL MONITORING
- Our skilled and highly trained clinical research associates (CRAs) ensure the highest quality review of data and effective interaction with study sites. Our CRAs conduct on-site monitoring visits throughout the study to: Oversee data collection, review source documentation and case report forms, ensure regulatory compliance, and resolve data queries as requested by clients.
- Thera Research is the CRO that takes responsibility. Through our vast knowledge of investigators and site dynamics, we build solid relationships with and fully support site personnel. Our experience enables us to understand the demographics of study participants in each therapeutic area and how to enroll them efficiently. Thera Research also understands how to identify high-enrolling sites and how best to work with them.
- Thera Research commitment to quality continues throughout the study. Senior-management oversight ensures that study challenges are anticipated and resolved proactively. With an emphasis on communication and team building, we ensure that all project-team members are fully informed on study progress. In every study that we conduct, our process is aimed at developing a long-term relationship with sponsor and sites.
- To start your next clinical study, contact Thera Research, the CRO that takes responsibility for driving and supporting sponsor and site staff. Thera Research clients benefit with reduced study timelines and enhanced study success.
- Experience in internal and external audits (Regulatory Authority / ISP).