Ayurvedic Third-Party Manufacturing in India
GMP-certified, end-to-end manufacturing for your Ayurvedic and nutraceutical products. From custom formulation to finished product delivery — under your brand name.
What is Third-Party Manufacturing?
Third-party manufacturing (also called contract manufacturing or toll manufacturing) is a business model where a brand outsources the production of its products to a specialised manufacturer. The manufacturer handles raw material sourcing, formulation, production, quality control, and packaging — while the brand focuses on marketing, sales, and distribution.
For Ayurvedic and nutraceutical brands, this model offers significant advantages: you get GMP-certified products without the massive investment of building and maintaining your own facility, and you can scale production up or down based on market demand. Third-party manufacturing is the most popular business model in the Indian Ayurvedic and nutraceutical industry, enabling hundreds of brands to launch and grow without factory ownership.
At Nutriley Healthcare, our third-party manufacturing service is fully comprehensive — we handle every aspect from custom R&D to final dispatch, with complete documentation and quality assurance at every step. Our facility is equipped with dedicated production lines for tablets, capsules, syrups, oils, powders, and cosmetics, ensuring your product gets the focused attention it deserves.
Trusted by brands including Dabur, Kapiva, and 100+ more, Nutriley is India's reliable manufacturing partner for Ayurvedic medicines, dietary supplements, and herbal cosmetics. Whether you are a startup launching your first product or an established brand looking for a reliable manufacturing partner, our third-party manufacturing service provides the quality, compliance, and scalability you need.
Ready to start? Call us or send an enquiry — we respond within 24 hours.
+91-7056015557Get a Free QuoteFormats We Manufacture
A wide range of dosage forms and product formats — all manufactured at our GMP-certified facility
Tablets
Plain, coated, chewable, effervescent — all tablet formats for Ayurvedic and nutraceutical formulations
Capsules
Hard gelatin and vegetarian capsules, including soft gel capsules for oil-based formulations
Syrups & Liquids
Ayurvedic syrups, tonics, juices, and liquid formulations in various bottle sizes
Herbal Oils
Medicated oils, massage oils, hair oils, and essential oil blends using traditional Ayurvedic methods
Churna & Powders
Classical Ayurvedic churnas, protein powders, herbal blends, and sachet-pack powders
Drink Mixes
Health drink mixes, superfoods, instant powders, and effervescent tablet formulations
Herbal Cosmetics
Creams, serums, face wash, shampoos, conditioners, and body care products
Custom Formats
Have a unique dosage requirement? Our R&D team can develop custom formats to your specification
How Third-Party Manufacturing Works at Nutriley
A transparent, step-by-step process designed to get your product to market as efficiently as possible
Initial Consultation
You share your product concept, target health claim, market (India/UK/USA), and approximate quantity. Our team schedules a free 30-minute consultation call to understand your requirements in detail and suggest the best formulation approach.
Formulation Development
Our in-house R&D team develops a custom Ayurvedic or nutraceutical formulation based on your requirements. We provide ingredient sourcing details, INCI names, and a detailed formula sheet for your review and approval.
Sample Production
We produce lab samples and pilot batch samples for your physical review. Samples are dispatched to you within 2-4 weeks. You test and provide feedback — we refine until you are 100% satisfied.
Regulatory & Compliance
We assist with FSSAI registration, product labelling compliance (India), FDA documentation (USA), and CE marking (Europe). All batch documentation, stability data, and microbiological test reports are prepared at this stage.
Full-Scale Manufacturing
After sample approval and regulatory clearance, we proceed to full-scale GMP-certified production. Multi-stage in-process quality checks ensure every batch meets specification. Complete batch records are maintained.
Packaging, Labelling & Dispatch
Products are filled, sealed, labelled (with your branding), packed into shipping cartons, and dispatched. We provide Certificate of Analysis (COA) for every batch. Delivery to India, UK, and USA with tracking.
Why Choose Nutriley for Third-Party Manufacturing
Multi-Certified Facility
Our manufacturing facility holds GMP, ISO 9001:2015, ISO 13485:2016, HACCP, FSSC, FSSAI, FDA, and CE certifications — ensuring your products meet international standards across all markets.
Authentic Ayurvedic Expertise
Founded with deep expertise in traditional Ayurvedic methods — herb grinding, decoction, Bhavana Dravya — we deliver authenticity that mass manufacturers cannot match.
In-House R&D
Our dedicated R&D lab handles custom formulation development, stability testing, and product innovation — saving you the cost of outsourcing your R&D to a third party.
100+ Brands Served
From industry giants like Dabur and Kapiva to ambitious startups — 100+ brands have trusted Nutriley for their third-party manufacturing needs since 2019.
Export-Ready Manufacturing
With offices in India, UK, and USA, we provide complete regulatory compliance support for international market entry — a capability most Indian manufacturers lack.
Fast Turnaround
Our streamlined processes ensure samples within 2-4 weeks and production batches within 4-8 weeks of approval — getting your product to market faster than competitors.
Third-Party Manufacturing FAQs
We offer flexible MOQs to accommodate brands at every stage. Our MOQs are designed to be accessible for startups while remaining scalable for larger brands. Contact us with your specific product and we will provide MOQ details and pricing.
Yes, absolutely. Our in-house R&D team specialises in custom Ayurvedic and nutraceutical formulation development. We develop formulations based on your health claims, target audience, and regulatory requirements. Full formula ownership is transferred to you after development.
Timeline varies by product complexity. Sample development typically takes 2-4 weeks. After sample approval and regulatory clearance, production batches take 4-8 weeks. We provide a project timeline during your initial consultation.
Yes. We have dedicated offices in London, UK and St. Petersburg, Florida, USA. Our manufacturing facility holds FDA (US) and CE (Europe) certifications, and we provide complete regulatory documentation support for international market entry.
We provide Certificate of Analysis (COA) for every batch, complete batch manufacturing records, microbiological test reports, stability data, and MSDS sheets where applicable. All documentation meets GMP requirements for Indian and international markets.
Ready to Manufacture Your Product?
Get a free consultation and quote within 24 hours.