• Develop a Strategy

Our team will work with you to identify the best possible approach to capture your most significant clinical outcomes through professionally selected clinical analyses.

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• Establish Budget and Timelines

Clinical trials can be costly and time-consuming but our team will work to ensure you stay within your clinical research budget and remain constantly aware of transparent timelines throughout the whole process.

• Review Protocol

A well-designed protocol is critical to achieve your goals on time and within your budget. Let us help you identify the most efficient way to conduct your trial. 

• Obtain Approvals

We will manage regulatory submissions to gain IRB approval for your trial.

• Recruit Subjects

Recruitment is one of the most challenging aspects of a trial. We oversee the finding of quality research subjects.

• Conduct Study

Our professionals at the clinical site in the Houston will work to conduct your study with the highest regard for participant safety, data quality and ICH-GCP compliance.

• Produce Reports

We prepare detailed reports appropriate for a medical literature reading audience. Our reports explain your research and findings and can be used for your publications. 

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• Substantiate Claims

Health claims made on natural health products must be supported by sound clinical research and are crucial to successful product development and marketing.

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