YOUR PARTNER FOR END-TO-END FULL-SERVICE CLINICAL TRIALS

We support your aspirations to bring life-saving medicines to market through well-managed clinical trials. With over 30 years of experience in conducting clinical trials, we understand your key challenges and have established systems to run a successful trial. Right from phase I to phase IV, we support your organization from startup to closure, and beyond, with our regulatory insights and quality approach. Our services are backed by technology & analytics that are developed specifically to meet the challenges you face daily, giving you the competitive edge.

SYETA LIFE SCIENCES GUARANTEE

• Patient Centricity
• Ensured Compliance
• Assured Quality
• Improved Collaboration
• Cost Optimization

SYETA Life Sciences leverages its domain expertise, technology knowledge, and world-class systems & processes to support your needs. Our end-to-end clinical trials operations provide you support with Clinical program management, feasibility, site selection and activation, Patient recruitment, Site management and clinical monitoring (including Risk Based Monitoring (RBM), Central Monitoring (CM), Remote Monitoring (RM) & Adaptive monitoring). We also offer you the advantage of our expertise in Medical Imaging, Bioavailability & Bioequivalence (BABE) studies, Bioequivalence pharmacokinetic (BE PK) and Bioequivalence clinical endpoint (BE CE), Biosimilars, and Non-Interventional Studies (NIS).

RELY ON OUR PROVEN EXPERTISE FOR SUCCESSFUL OUTCOMES FOR YOUR NON-INTERVENTIONAL STUDIES

Non-Interventional Studies (NIS) are helpful to examine the safety, tolerability and effectiveness of your medical product in market. Important findings like drug interactions, side effects, patience compliance, quality of life improvements and much more may be discovered through NIS. Such findings enable you to leverage your product to the maximum and improve the lives of patients.

Most NIS do not follow a unified protocol, requiring specialized skills to run a NIS trial. Running such trials requires expertise in handling real-world situations, and dealing with tricky situations like patient non-compliance, inaccurate dosing or application. Source data collection across multiple health centers is also tricky and many a time, data from NIS trials are inconsistent, non-homogeneous, and even missing!

SYETA Life Sciences is Your Partner in Non-Interventional Studies

• Experience
• Expertise
• Technology
• Approach
• Processes
• Quality

We Support Your End-to-End NIS Requirements

Study Design : Design & plan your prospective or retrospective study with our experts to ensure successful outcomes

Study Conduct : Your non-interventional studies are conducted in real life situations, requiring the right experience and expertise for successful completion

Data Standardization & Analysis : Expert biostatisticians are available to standardize and analyze your study data

Regulatory Submissions : Our regulatory submissions services are backed by a cutting-edge technology platform that enables first-time-right submissions and follow ups.

Pharmacovigilance : Bring patient safety to the forefront with our expert pharmacovigilance services and systems

Study Closure : Well-handled study closures with focus on data cleaning; country, and site closure procedures, Final QC of files, and publications