Clinical Research Services

Clinical Research Services

Clinixir offers end-to-end solutions for all your clinical research needs. Clinixir can be your ideal partner and guide throughout every step of your clinical trial, from scientific and regulatory support to compliance, pharmacovigilance, site engagement, and data management.

Our expert staff, state-of-the-art facilities, and bespoke services enable you to enhance patient engagement, reduce risk, and gain higher quality data, all towards the ultimate goal of developing better treatments and improving patient outcomes.

We provide

Clinical Trial Planning & Design

Providing scientific and regulatory advice to support protocols and clinical development.

Feasibility, Regulatory & Startup

Assessing the activities and documentation at a research site to ensure protocols and SOPs are followed correctly.

Clinical Monitoring

Overseeing the progress of a clinical trial as well as ensuring that it is conducted, recorded, and reported in accordance with protocols, SOPs, and regulatory requirements.


Patient Safety Solutions and Medical Monitoring that meet and exceed global standards.

Project Management

Managing activities of personnel engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives, which include planning, directing, and coordinating projects.

Site Engagement

Solutions to drive start-up, recruitment, quality, and timelines at Clinixir partner sites.

Data Management

Collection and processing of patient data as part of a clinical trial, with all e-clinical systems complying with US FDA’s 21 CFR Part 11 requirements.


Providing operational and strategic statistics needed for every aspect of drug development to determine efficacy and effectiveness in clinical trials.

For more information

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