
For over 25 years, Vedic Lifesciences has been a trusted global partner for evidence generation and innovation.
We combine scientific design excellence, regulatory strategy, and executional speed to help health product innovators prove, publish, and promote their claims with confidence.
To empower innovators through credible science, compliant claims, and clinically proven outcomes.

To be the world's most trusted innovation and regulatory partner for consumer health, borderline and other under-served categories.

Access To India's Diverse Population With Multi-Regional Study Capabilities (US, EU, Australia, APAC)

Preferred Research Partner To Leading Health Products & Brands Worldwide
High Acceptance Rates In Credible Peer-Reviewed Journals

End-To-End Clinical Operations With Global Reach
Adaptive Trials, Hybrid Trials,
Decentralized Models

Beyond Execution; Your Scientific Intellectual Partner

Experience With USFDA, Health Canada, EFSA, TGA, MFDS
One Of The Few CROs Globally With Deep Natural Product Expertise

Trusted By Top Brands Across Continents & Regulatory Regions

GCP-Compliant Sites, Accredited Labs, Robust Data Integrity
Recognized By Industry Leaders For Scientific Credibility & Excellence
Our team combines deep expertise with a client-first approach — ensuring every study delivers value, compliance, and credibility.
Guiding your studies with 25 years of scientific & regulatory expertise. Directly accessible to ensure your voice shapes our solutions.
With 25 years of leadership at Vedic, Jayesh blends scientific rigor with customer-centric vision. A pharmacist trained at the University of Minnesota, he ensures study designs align with global regulatory norms (FDA, EFSA, TGA, FSSAI & more). Clients value his direct accessibility, hands-on involvement at trade shows, and ability to turn feedback into continuous improvement. Jayesh also founded Enovate Biolife, now part of OmniActive, and guides brands in building proprietary science-backed success stories.
Your trusted partner for costs, contracts & strategy alignment. Champion of evidence-based claims and client success.
Kriti is your go-to partner for navigating costs, contracts, and strategy shifts. A pharmacist with an MBA in marketing and past experience with large pharmaceutical firms like Sun Pharma, she ensures every client’s commercial and regulatory needs are aligned. With 7+ years at Vedic, she brings empathy for branded ingredient providers and champions evidence-based claims. A member of WIN and guest host of Nourish & Navigate, Kriti makes collaboration seamless and future-focused.
Designing robust, realistic studies that deliver credible results. Keeping your trials audit-ready and scientifically sound.
He leads clinical research at Vedic, including site operations, scientific writing, medical monitoring, CDM, statistics, trial supplies, etc. Dr. Sanjay ensures your studies are designed for robust, real-world results. With decades of experience in clinical trials, bioavailability studies, and FDA audit readiness, he leads operations, medical writing, stats, and IP supplies. Clients appreciate his ability to spot risks early, keep studies on track, and deliver with scientific integrity. Beyond work, his passion for sports, photography, and books fuels his versatile perspective.
Safeguarding your research with independent, GCP-compliant audits. Ensuring every study is accurate, reliable & regulation-ready.
For 16+ years, Anil has been the guardian of quality at Vedic. His team independently audits every study — sites, vendors, and processes — ensuring strict ICH-GCP compliance. Thanks to his leadership, Vedic is CDSCO-registered and ISO:9001 compliant, giving clients confidence that every protocol deviation is flagged and corrected swiftly. With Anil’s oversight, your study comes with built-in assurance. He also heads the preclinical and toxicology department with efficiency and grace.
Transforming traditional wisdom into market-winning claims. Helping you position products with strong, compliant science.
Sachin bridges traditional wisdom with modern science. An Ayurvedic doctor and clinical researcher with Johnson & Johnson experience, he helps clients design studies that uniquely position their products. From shaping endpoints to identifying credible claims, his expertise ensures your innovation stands out while staying compliant.
Turning your research needs into scalable growth solutions. Driving global studies, DCTs & medical device innovations.
Sameer is a strategic leader transforming research into real-world impact. With extensive experience driving global studies, decentralized clinical trials (DCTs), and medical device innovations, he ensures operational excellence across teams and geographies. His leadership blends precision with innovation — delivering scalable, compliant, and impactful research outcomes.
Running large-scale trials with operational precision. Specialist in gut-health studies that deliver reliable, scalable insights.
Dr. Sonal leads clinical operations for high-volume studies, with deep experience in gut-health and joint health studies. She ensures participant recruitment, site coordination and logistics are efficient and scalable so your study meets timelines and quality expectations. Clients benefit from her pragmatic planning, on-ground problem solving and commitment to data completeness.
Transforming traditional wisdom into market-winning claims. Helping you position products with strong, compliant science.
Amit heads our medical writing team and ensures study protocols, clinical study reports and manuscripts are scientifically rigorous, regulatory-ready, and publication-focused. He helps translate complex data into compelling narratives that support regulatory claims and scientific visibility — accelerating your route to credible publications and market trust. He also leads the way for the medical monitoring, data management and statistics teams.
Clinical oversight that protects data integrity and participant safety.Rigorous medical review from screening to final report sign-off.
Dr. Ishan reviews every participant report against protocol I/E criteria and provides final medical adjudication, ensuring clinical decisions are robust and defensible. With prior experience at Pfizer and expertise in medical communications strategy, he combines strict clinical oversight with clear medical interpretation — reducing regulatory risk and strengthening study credibility. He also looks into designing and estimating costs and timelines for new study requests.
Hiring and retaining the talent that delivers your study outcomes. Decade and a half-long stewardship of people, processes and project continuity.
Abhishek ensures Vedic recruits and retains experienced staff who can execute complex trials reliably. By building teams with the right skills, he helps guarantee continuity, high operational standards and on-time delivery for your projects. If you’re recruiting or partnering, Abhishek is the internal contact who keeps people performance aligned to your study goals.
Transparent, practical financial guidance for smarter study investments. Protecting budgets while enabling the science you need to grow.
Shilpa manages financial strategy and commercial structures so your study budget is optimized without compromising scientific quality. She offers clear costing, flexible commercial options, and proactive budget risk management — helping clients plan studies that are financially sustainable and deliver measurable ROI.
We operate under ICH-GCP, GLP, and ISO-certified quality systems.
Our research is compliant and audit-ready for FTC, FDA, EFSA, KFDA, TGA and Health Canada standards.






From strategy to compliance, our team is here to make your science stronger.
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