RHETT HEALTHCARE
Care beyond cure, always and in all ways!
Who We Are
You Dream, We Formulate. We Deliver.
At Rhett Healthcare, our motto is more than just words — it's the foundation of everything we do. As a leading USFDA-registered, WHO-GMP certified Contract Development and Manufacturing Organization (CDMO), we specialize in turning your product vision into world-class, high-efficacy nutraceutical formulations.
From formulation to finished dosage forms, we follow a strict GMP culture that goes beyond compliance. Our processes are engineered for precision, consistency, and quality — the first time, every time.With unwavering passion, purpose, and partnership, we deliver solutions that make a difference in every capsule, powder, tablet, and herbal extract.
Together, We Make Miracles.
The Rhett Mission
You dream, we formulate.
Rhett Healthcare, a premier contract development and manufacturing organization located in the Biotech Park of Hyderabad, India, is committed to the highest standards of manufacturing practices. As a GMP-compliant company, we hold various certifications that underscore our dedication to quality and safety in all operations.
Rhett Healthcare specializes in providing top-tier healthcare and lifestyle products, proudly holding prestigious accreditations from NSF, ISO, WHO GMP, NOP, NPOP, FSSAI, and USFDA, among others.
Our state-of-the-art facility includes Rhett Herbals, our in-house extraction plant, exemplifying our commitment to backward integration. This setup ensures the highest authenticity and quality of herbal extracts, which are meticulously manufactured and tested using High-Performance Liquid Chromatography (HPLC) for assay.
Eurofins Certification – 21 CFR Parts 111 & 117 Compliance
Rhett Healthcare Pvt. Ltd. is proud to be certified by *Eurofins* for compliance with *US FDA 21 CFR Part 111 (Dietary Supplement cGMP)* and *21 CFR Part 117 (Food Safety Modernization Act – FSMA)*. This certification reflects our unwavering commitment to quality, safety, and regulatory excellence across our manufacturing operations .
What This Certification Means
The 21 CFR Parts 111 and 117 regulations are among the most stringent global standards governing dietary supplements and food manufacturing. Certification by Eurofins—an internationally recognized testing, inspection, and certification body—confirms that our facility, processes, and controls meet these rigorous US FDA requirements.
Our certification covers the manufacturing of *capsules, tablets, powders, and resins*, along with a wide range of technologies including formulation, encapsulation, coating, mixing, packaging, labelling, warehousing, and controlled heating processes .
Why This Is Important for Our Partners & Customers
* *Regulatory Confidence*
Ensures full alignment with US FDA cGMP and FSMA requirements, supporting smooth market access for domestic and international clients.
* *Assured Product Safety & Quality*
Demonstrates robust quality systems, validated processes, and strict hygiene and safety controls throughout production.
* *Global Market Readiness*
Enables brands to confidently export and distribute products in highly regulated markets such as the United States.
* *Operational Transparency*
Validates traceability, documentation, risk-based food safety controls, and preventive systems across our facility.
* *Trusted Third-Party Validation*
Certification by Eurofins reinforces trust with regulators, brand owners, and end consumers alike.
Our Commitment
This certification is not just a milestone—it is a reflection of our continuous commitment to *world-class manufacturing standards, regulatory compliance, and customer success*. At Rhett Healthcare Pvt. Ltd., quality and safety are embedded into every stage of our operations, ensuring reliable, compliant, and high-quality products for our partners worldwide.
