We at ClinSync, have a strong expertise to design, develop and execute early development programs that allow clients to make right decisions, increase efficiencies and reduce timelines.
We have a strong clinical expertise and strategy at an early phase stage which is critical to long-term clinical success. As a full service early stage CRO that is not only capable of providing the clinical conduct of your studies, but had the ability to provide all round end to end services which ensures right evidence is collected to help you move to the next step.
First-in-Man Programs (SAD + MAD (NBE Indian client) + FE + CYP450 Interaction)
Microdosing studies
Clinical PK/PD studies
Imaging (PET, fMRI) studies
Bioavailability/ANDA studies
Bioequivalence/ANDA studies
Vaccine studies
Cardiac Safety/Thorough QT/QTc studies
Drug-Drug Interaction studies
PK bridging studies for Market Formulation Vs Final Market Image Formulation Vs Clinical Trial Formulation- Rectal foam studies, Fecal Biomarker study, Renin-angiotensin biomarker study, Pharmacoscintigraphic Imaging, Intramuscular or sub-cutaneous injection studies.
Review of Preclinical Data
Design and Preparation of the Trial
Clinical Project Management
Preparation of the Study Protocol, Informed Consent, and Case Report Forms
Clinical Conduct
Clinical Data Management
Biostatistics
Bioanalysis
Conduct PK/PD and/or Pop PK/PD Data Analysis and Modeling
Prepare PK/PD Report
Prepare and publish Fully Integrated Clinical Study Reports
Monitoring
Safety Monitoring