JOIN A CLINICAL TRIAL
JOIN A CLINICAL TRIAL

Innovative Virtual Trials

Revolutionizing Research with Flexible, Real-World Solutions

PARTICIPANT-REPORTED OUTCOMES VIRTUAL TRIALS (PRO-VT™)

KGK’s Participant Reported Outcomes Virtual Trials (PRO-VT™) offers a swift, cost-effective solution to validate the efficacy of your nutraceutical products, bringing innovation and efficiency to the forefront of your research.

Why Choose KGK Science?

  • Decades of Expertise: Benefit from 27 years of trial experience ensuring reliability and accuracy.
  • Participant-Reported Outcomes (PROs) Support: Our trials validate participant-reported claims, meeting HIPAA and 21 CFR Part 11 compliance for privacy and risk mitigation.
  • Reliability Guarantee: Ensure dependable virtual trial outcomes with evaluation of Adverse Events (AEs) and product compliance, delivering accurate and safe results.
  • Regulatory Support: Craft federally compliant claims for seamless market entry.
  • Sample Size: Efficient trial design with sample sizes of 250, 500, or more.
  • Swift Reporting: Rapid reporting tailored for C-suite executives for prompt decision-making.
  • Consumer Insights: Optional Consumer Report Card for individual participant responses, enhancing product efficacy understanding.
  • Affordable Intellectual Property: Secure affordable IP rights on innovative ingredients and products.
  • Data Ownership: Retain ownership of trial data for control and confidentiality.
  • Substantiation Support: Initial support for fundraising rounds, bolstering investor confidence.
  • Accelerated Timelines: Fast timelines for M&A deals, enhancing business agility and opportunity realization.

CUSTOMIZED VIRTUAL TRIALS (C-VT™)

Our Premier Customized Virtual Trials (C-VT™) offer meticulous control, conducted remotely with a robust design to meet regulatory standards and serve as a seamless alternative to in-person clinical trials.

Benefits of Customized Virtual Trials:

  • Tailored Design: Customize trials based on your specific claims, product goals, or safety objectives.
  • Expanded Participant Pool: Allows individuals to enroll remotely, removing geographical barriers that limit traditional in-clinic trials.
  • Flexibility in Data Collection: Customize trial parameters to accommodate diverse study needs.
  • Regulatory Support: Craft federally compliant claims for seamless market entry.
  • Sample Size: Efficient trial design with large sample sizes.
  • Expanded Scope: Options for additional features such as biological sample collection and wearable data devices to enhance study data, along with compliance calls for direct participant communication to improve safety monitoring, ensure IP compliance, and reduce participant attrition.
  • Unlimited Indications: Explore a wide range of therapeutic areas and conditions.
  • Adaptable Trial Models: Choose between completely remote or hybrid in-clinic/virtual models.

Journal Selection and Submission:

  • Strategic Journal Selection: We assist in identifying the most suitable peer-reviewed journals for your study, prioritizing high-impact publications.
  • Compliance Assurance: Manuscripts are meticulously prepared to meet the specific formatting and submission guidelines of each journal.

KGK Science has been delivering top-notch clinical research trials and expert regulatory support for the nutraceutical, cannabis, hemp, and psychedelic industries for over 27 years, aiding companies in bringing their products to global markets with custom trials and claim substantiation strategies.

Quick Links

Head Office Address

275 Dundas St., Suite G02
London ON N6B 3L1


Clinic Hours

Monday - Saturday 7:00 AM - 3:00 PM

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