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Clinical Trials

We Help in Conducting Evidence-based Research

Laboratory
Laboratory

We adapt clinical trials to individual requirements

CardioVerse provides clinical trials for companies of various sizes, including multinational conglomerates and startup companies. We facilitate the easy and low-cost generation of product claims supported by evidence. We know how to develop and execute clinical trials on a tight budget without sacrificing quality or efficiency in any way. We are committed to keeping you informed at every stage of the clinical trial process in an effort to provide the smoothest and most successful experience for you.

Analysing data

What is a clinical trial?

Clinical trials are the gold standard of scientific evidence. Health claims about products may need to be backed up with evidence from clinical trials. When done correctly, they offer your product's most substantial and validated sacrifice proof. Several essential considerations need to be made in designing a clinical trial to guarantee that the study's
goals will be attained and that the data obtained will apply to the claimed benefits of
your product. 

Analysing data
Sorting Medicine

Clinical Trails at CardioVerse

We are committed to providing our clients with the highest quality research services, delivered with integrity, transparency, and innovation. We are dedicated to building long-term relationships with our clients based on trust, collaboration, and a shared commitment
to achieving success.

How Are Clinical Trials Done at CardioVerse?

From the very beginning of your research until the end of your trial, CardioVerse will take care of your needs. Depending on the specifics of your clinical research, you can pick and choose from the range of services we offer. And in the end, we will provide you with a detailed scientific report. And we are also very cost-effective!

01

Study Conceptualization

  • Developing the Research Question

  • Hypothesis Development 

  • Study Design

  • Sample Size Calculation

02

Study Execution

  • Protocol Development

  • Informed Consent Form (ICF) Development

  • Institutional Review Board Process

  • Registering the Study in ClinicalTrails.Gov

  • Participant Recruitment

  • Participant Retention

03

Data Management and Analysis

  • Use of Validated Instruments to Capture Data

  • Effective Data Collection

  • Effective Data Management

  • Data Analysis

04

Dissemination of Study Results

  • Creating the Final Report

  • Publishing in Peer-reviewed Journals

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