Areas of expertise

Clinixir’s expert researchers bring unparalleled excellence to a wide variety of research fields. With a comprehensive track record of conducting trials across multiple disciplines, we possess the expertise needed to develop and implement study designs tailored to the specific needs of each area of medical innovation.

Whether it be oncology, infectious and rare diseases, neurology, metabolic diseases, herbal medicines, medical devices, or other innovative areas of medical research, our team applies its deep knowledge and experience toward developing clinical solutions that meet the highest international standards. With our team of experts by your side, you can be confident in the quality and efficacy of your research, ensuring that your innovations make a meaningful impact on society. 

Oncology

Oncology clinical trials require a committed team with professional experience in every aspect, facet, and stage of cancer. From radiation oncologists, to surgeons and investigators, experts on cancer research can ensure the successful progression of each clinical trial.

At Clinixir, we guide and support you through your oncological clinical trials with biostatistical analysis. In addition, our experts in their respective fields can develop the right protocols and support for your trials. We provide you with all-encompassing clinical project management services so that your oncology trials meet their timelines and objectives without failure.

We are a reliable one-stop service provider for your clinical research needs. Whether it’s providing you with a complete team to handle all matters related to project management, medical writing, regulatory affairs, site management, or clinical monitoring for a wide range of cancer types, you can be sure to receive our full attention for your oncological trials.
We are also partnered with 8 of Thailand’s leading medical institutions who provide us with additional expert input from top clinical research professionals, further ensuring that your study designs and protocols are ideally structured and meet every regulatory requirement prior to trial commencement. By drawing from this wide range of preclinical experience in oncology, we can deliver fast-track development so that you can conduct your patient studies as soon as possible.

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