Nutraceutical supplements and healthy foods - Clinical Research

Scientific Validation & Compliance

At Genesys Scientific, we deliver gold-standard testing and clinical research services for the nutraceutical industry. We ensure your products meet global safety benchmarks, including FSSAI, USFDA, and EFSA guidelines.

From molecule to market, our integrated approach combines analytical chemistry with clinical expertise to prove efficacy, ensuring your brand stands on a foundation of trust and verifiable science.

Nutraceutical Research Services

Comprehensive clinical testing and regulatory compliance for nutraceutical products

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Nutraceutical Research

Comprehensive clinical validation and safety testing for dietary supplements, functional foods, and nutraceutical products with regulatory compliance.

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Real World Evidence (RWE)

Leveraging real-world patient data to generate clinically meaningful insights that drive product improvement and healthcare outcomes.

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Phase I-IV Clinical Trials

Complete clinical trial management from Phase I safety studies through Phase IV post-market surveillance with expert protocol design.

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Medical Writing

Professional medical writing services for clinical study reports, regulatory submissions, manuscripts, and scientific publications.

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Observational Studies

Longitudinal observational research to gather real-world data on treatment effects and patient outcomes in diverse populations.

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Case Studies

Detailed case study analysis and documentation for clinical outcomes, adverse events, and unique patient responses to treatments.

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Clinical Publications

Expert support for publishing clinical research in peer-reviewed journals, including manuscript preparation and journal selection.

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Regulatory Insight

Strategic regulatory guidance and compliance support for FSSAI, USFDA, EFSA, and other international regulatory submissions.

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Pre-Clinical Studies

Comprehensive pre-clinical testing including toxicology, pharmacokinetics, and safety assessment before human trials.

Ayurvedic herbs and traditional medicine - Clinical Research

Modernizing Traditional Wisdom

Genesys Scientific bridges the gap between ancient Ayurvedic texts and modern clinical requirements. We specialize in evidence-based validation of herbal formulations under AYUSH and international standards.

Our specialized protocols respect the holistic nature of Ayurveda while applying rigorous scientific methodologies to establish safety, standardization, and therapeutic efficacy.

Ayurvedic Research Services

Evidence-based validation of herbal formulations under AYUSH and international regulatory standards

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Ayurvedic Research

Scientific validation of traditional Ayurvedic formulations with modern clinical methodologies and regulatory compliance.

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Phase I-IV Herbal Trials

End-to-end clinical development for herbal drugs from safety testing to large-scale therapeutic confirmation studies.

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Observational Studies

Long-term observational research on Ayurvedic treatments to gather real-world efficacy and safety data.

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Safety & Efficacy Studies

Detailed toxicological studies and efficacy trials to prove the safety profile of poly-herbal formulations.

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Herbal Standardization

Ensuring batch-to-batch consistency and active marker profiling for reproducible clinical results.

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AYUSH Compliance

Expert guidance for AYUSH regulatory submissions and compliance with traditional medicine standards.

Why Choose Genesys Scientific?

Your trusted CRO partner for clinical research excellence

Regulatory Expertise

Full compliance with FSSAI, USFDA, EFSA, and AYUSH regulatory standards

15+ Years Experience

Proven track record in clinical research and product validation

Expert Team

Highly qualified researchers, clinicians, and regulatory specialists

Fast Turnaround

Efficient study execution with quality-focused timelines

Ready to Start Your Clinical Research Project?

Contact us today for expert CRO services and regulatory compliance support

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