Simple and elegant solutions to complex challenges At Clinhealth, we believe in a meaningful and agile approach towards supporting our clients’ clinical trial management requirements.

We have the capability to lead and partner right from the stage when a research question is being formulated to the stage of publication At Clinhealth, we understand that while non-industry funded clinical trials need to be conducted with adherence to the highest standards of quality, delivery and regulatory compliance, the CRO services must be affordable and meaningful. We partner with individual physician investigators, academic and research institutions and other non-industry stakeholders to create and deploy clinical trial solutions that are highly customized and unique to each situation. At Clinhealth, we have deep expertise in supporting end-to-end delivery of Investigator Initiated Trials. Our experts bring valuable insights at every stage of the process. Contact us through the form below and one of our experts will be in touch with you right away.

Regulatory requirements worldwide are continually evolving and differ from one country to another.

Clinhealth provides its clients an experienced and cohesive regulatory, and toxicology expert team with extensive experience of major regulatory agencies for drug and device clinical trials.

The regulatory and clinical teams have expertise in small molecule drugs, medical devices, vaccines, cellular therapies, immunotherapies, monoclonal antibodies, peptides and recombinant protein products.

Informed Decisions for Meaningful Outcomes Having supported a range of clinical trials with different levels of complexity, our teams have the experience and expertise of not only executing clinical studies but also to advise clients along the clinical development pathway. We have the capability to support clients through the decision process from pre-clinical stage all the way to post-marketing stage of development.

Clinical trials are becoming increasingly complex, time and cost constrained, and competitive. In this challenging landscape, our clients are looking at the best way to navigate the challenges so as to reach the next milestone in the development process keeping timelines and budgets within plans. Our teams help in providing advice on how to utilize best practices, interpretation of guidelines and recommendations from regulatory agencies as well as clinical study designs so that key answers to reach the next stage of development are derived with the least amount of effort, time and cost. We do this through a collaborative work-process and advisory support from key experts.