Who We Are

Science for Restoration. Quality for Longevity.

Founded with the mission of manufacturing medicines of uncompromising quality, Sanatav Remedies has grown into a trusted pharmaceutical partner. We operate multiple advanced manufacturing blocks specializing in cardiovascular, anti-diabetic, neurology, and gastrointestinal therapeutics.

Our research team collaborates with leading universities and clinical research organizations (CROs) to formulate drugs that show superior bioavailability, simplified dosage administration, and fewer side effects.

20+ Years Research
WHO-GMP Certified
50+ Export Portals

Corporate Milestones

2006Foundation

Established first formulation research lab in New York.

2012WHO-GMP Compliance

Commissioned state-of-the-art manufacturing plant, certified for export.

2020Global Logistics Expansion

Connected 50+ international distributors via cold-chain tracking.

Our Mission

To research, formulate, and deliver accessible, high-potency therapeutics that restore patient health and empower clinical care providers worldwide.

Our Vision

To establish a global standard in pharmaceutical integrity, recognized as the most trusted partner in clinical formulation and healthcare safety.

Regulatory Audits & Compliance

Certifications & Standards

We understand that safety is paramount. Our chemical formulations and syntheses are regularly audited by international regulatory boards to guarantee consistent compliance.

WHO-GMP Certification

World Health Organization Good Manufacturing Practices

Certified since 2012

Regular international audits validate our batch processing cleanliness, document trails, and API storage parameters.

ISO 9001:2015 Standard

International Quality Management Systems

Certified since 2015

Certified frameworks for chemical analysis, logistics coordination, and administrative product traceability.

FDA Registration

U.S. Food and Drug Administration Facility Listing

Registered

Complies with active clinical manufacturing regulations and drug master file procedures.

ISO 14001:2015 Standard

Environmental Quality Management

Certified since 2018

Ensures pharmaceutical synthetic waste and energy utilization minimize carbon footprint.

Medical Advisory Board

Our Leadership & Scientific Panel

Meet the pharmacologists, regulatory experts, and medical professionals steering Sanatav Remedies towards safe, clinical innovations.

AP

Dr. Arthur Pendelton

Chief Scientific Officer (CSO)

Ph.D. in Molecular Pharmacology, Harvard University

Directs our core research facility, focusing on drug solubility, crystallization, and next-generation clinical trials.

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SJ

Sarah Jenkins, R.Ph.

VP of Quality Assurance & Compliance

M.S. in Pharmaceutical Chemistry, Oxford

Supervises our raw API intake verification, batch validation protocols, and WHO-GMP audit readiness.

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RM

Dr. Rajiv Mehta

Director of Pharmacovigilance & Clinical Safety

M.D. in Cardiology, Johns Hopkins University

Manages drug post-market surveillance, adverse effect logging, and patient-first safety advisory boards.

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