Specialised CLINICAL TRIALS

for Nutraceuticals & Dietary Supplements

Process

Journals

From Planning to Implementation

We provide a collaborative, transparent and customized path to conducting research.Let’s work together to elevate your brand!

Image showing the initial phase of a clinical trial for a food supplement: formulating research questions, defining study population, determining study duration, outlining endpoints, and establishing research protocol.

Development of Research Protocol

The initial phase in conducting a clinical trial for a food supplement involves formulating the research questions, defining the study population, determining the study duration, outlining the endpoints to be evaluated, and establishing the research protocol.

Image depicting researchers obtaining regulatory approval from authorities like the FDA in the United States or the EMA in Europe before commencing a clinical trial. This approval validates the ethical conduct and regulatory compliance of the trial.

Regulatory Authorization

Prior to commencing the clinical trial, researchers are required to secure approval from the relevant regulatory authorities, such as the FDA in the United States or the EMA in Europe. This approval ensures that the trial is conducted ethically and adheres to regulatory standards.

Image illustrating researchers recruiting participants for a clinical trial, which may involve healthy individuals or those with specific health conditions based on the research focus.

Image illustrating the process of participants providing informed consent before enrolling in a clinical trial, involving a thorough understanding of the study, its risks and benefits, and voluntary agreement to participate.

Informed Consent Process

Participant Recruitment

Subsequently, researchers undertake the task of recruiting participants for the clinical trial. Participants may include healthy individuals or those with specific health conditions, depending on the focus of the research.

Before enrolling in the clinical trial, participants are obligated to provide informed consent. This entails a comprehensive understanding of the study, including its potential risks and benefits, and a voluntary agreement to participate.

Image depicting participants being assigned to receive either the food supplement under investigation or a placebo/control as part of the clinical trial, following the study protocol for intervention administration.

Implementation of Intervention

Participants are then allocated to receive the food supplement under investigation or a placebo/control. The intervention is administered in accordance with the specified study protocol.

Image showing researchers collecting data on participant outcomes throughout the clinical trial, including health measurements, laboratory tests, surveys, and evaluations to track progress and results.

Data Collection Procedures

Throughout the duration of the clinical trial, researchers meticulously gather data on participant outcomes. This may involve various assessments such as health measurements, laboratory tests, surveys, and other evaluations.

Image illustrating rigorous monitoring procedures during a clinical trial to uphold participant safety and data accuracy. This includes regular check-ins, monitoring for adverse events, and ensuring data quality.

Ongoing Monitoring and Oversight

Rigorous monitoring is conducted during the clinical trial to ensure participant safety and data accuracy. This oversight includes regular participant check-ins, vigilance for adverse events, and assessments of data quality.

Data Analysis and Reporting

After analyzing the data using statistical methods to determine the significance of observed effects, researchers document their findings in scientific publications or conference presentations, summarizing study methods, results, and conclusions.

Based on Good Clinical Practice (GCP) guidelines

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Journals

We are selecting a strong reputation...

Publishing clinical study results on food supplements in reputable journals enhances transparency, credibility, and engagement with the scientific community. Researchers typically target peer-reviewed journals related to nutrition, pharmacology, or the specific study area for publication.

Our mission

Our Mission

Our mission is to establish your brand as safe, reliable, and trustworthy. We are committed to promote better outcomes for consumers through personalized clinical trials tailored

to your brand’s unique needs.

We conduct clinical trials without compromising on quality. We cooperate closely with medical personnel and doctors to ensure the safety and well-being of testing participants in clinical trials for food supplements.

Our team handles everything, from planning to implementation, and our transparent communication ensures you have the smoothest and most rewarding trial experience.

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