AYUSH Manufacturing Registration · GMP Certified · US FDA MoCRA

Nutraceutical Contract Manufacturing India: AYUSH Registered GMP Facility

Auriga Research provides nutraceutical contract manufacturing in India under our AYUSH Manufacturing Registration. The scope covers tablets, capsules, softgels, powders, sachets, liquids, and herbal formulations across vitamins, minerals, omega-3, protein, collagen, probiotics, and Ayurvedic supplements.

Manufacturing operates at our GMP-certified facility in Baddi, Himachal Pradesh, which is also registered with the US FDA under MoCRA. Our analytical and testing laboratories are NABL accredited under ISO/IEC 17025:2017 and support raw material, in-process, stability, and finished product release testing.

We support brand owners from formulation through commercial production. Documentation and export support are provided as per applicable regulatory requirements for your target market.

Get a Manufacturing Quote Call +91-7428116100

Dosage Forms and Packaging

Tablets, capsules, softgels, sachets, powders, sticks, and liquid preparations across the nutraceutical scope.

Nutraceutical product range, softgels, sachets, and bottles

Nutraceutical Dosage Forms

Softgels · Sachets · Tablets · Bottles · Sticks

Regulatory Pathways for Nutraceutical Claims

The most important decision before manufacturing begins is understanding which regulatory pathway applies to your product claim.

Nutritional and Efficacy Claims

Nutritional and efficacy claims for food supplements are handled under FSSAI guidelines, including the FSSAI Nutraceutical Regulations. Examples include claims such as "supports immune function" or "supports bone health" backed by appropriate substantiation evidence.

Disease Risk Reduction Claims

Disease Risk Reduction claims, which position the product at the food and drug boundary, require a full CDSCO clinical trial pathway. Examples include claims around reducing the risk of a specific disease.

Auriga will advise on the correct pathway for your product during the initial consultation, and align manufacturing, testing, and documentation accordingly.

Product Categories We Manufacture

Five primary nutraceutical categories supported across tablets, capsules, softgels, sachets, sticks, powders, and liquid preparations.

Vitamin and mineral tablets and capsules

Vitamins & Minerals

Single ingredient and combination vitamin and mineral products in tablet, capsule, effervescent, and sachet forms.

Omega-3 & Essential Fatty Acids

Softgels and liquid preparations of fish oil, flax seed oil, and other essential fatty acid blends.

Herbal & Ayurvedic Supplements

Classical and proprietary Ayurvedic formulations, single-herb and polyherbal supplements manufactured under AYUSH registration.

Protein and sports nutrition powder sachets

Protein & Sports Nutrition

Whey protein, plant protein blends, amino acid sachets, and sports nutrition powders in jars and sachet formats.

Collagen & Probiotics

Hydrolysed collagen sachets and sticks, probiotic capsules and sachets with strain identity and CFU support.

Who Engages Auriga for Nutraceutical Manufacturing

Nine buyer profiles use our nutraceutical contract manufacturing service.

Nutraceutical Brands Launching in India

Brands launching new supplement products in the Indian market and looking for a manufacturing partner that handles formulation, testing, and production.

Health & Wellness Brands

Health and wellness brands looking for a GMP manufacturing partner with integrated analytical and stability testing support.

AYUSH Supplement Companies

Companies developing classical and proprietary Ayurvedic supplements that need AYUSH-registered manufacturing.

D2C Wellness Founders

Direct-to-consumer wellness founders launching tablets, capsules, sachets, and powders through e-commerce and modern retail.

Startup Brands Launching New Products

Early-stage nutraceutical brands launching their first SKU and looking for a partner that supports them from formulation through commercial production.

Established Brands Expanding Portfolios

Existing brands adding new product lines or extending into adjacent supplement categories and looking for additional manufacturing capacity.

Pharma Companies Entering Nutraceuticals

Pharmaceutical companies extending into nutraceutical, health supplement, and wellness categories and looking for a partner familiar with pharma quality standards.

Private Label Businesses & Retail Chains

Retailers, distributors, pharmacy chains, and supermarket chains building their own private label nutraceutical ranges.

Export Brands

Brands producing nutraceuticals for export markets and needing manufacturing partners that can provide documentation as per applicable regulatory requirements.

Why Auriga for Nutraceuticals

Six reasons brands choose Auriga as their nutraceutical manufacturing partner.

AYUSH Manufacturing Registration

Manufacturing operates under our AYUSH Manufacturing Registration, which is the appropriate route for the Ayurvedic, herbal, and traditional knowledge nutraceutical categories Auriga produces.

GMP Certified Facility

Our manufacturing facility in Baddi, Himachal Pradesh is GMP certified, with documented batch records, in-process controls, and a finished product release process.

US FDA MoCRA Registered

The facility is registered with the US FDA under the Modernization of Cosmetics Regulation Act, which supports brands manufacturing personal care and cosmetic nutraceutical products with US distribution scope.

In-House Testing via NABL Laboratories

Our analytical and testing laboratories are NABL accredited under ISO/IEC 17025:2017. Raw material, in-process, stability, and release testing run alongside the manufacturing operation. NABL accreditation applies to the testing laboratories, not to the manufacturing facility.

Integrated Formulation Development

Formulation development is available through the same group, so a single relationship covers idea, formulation, testing, and manufacturing.

Low MOQ, Flexible Batch Sizes

We support pilot, small commercial, and full commercial batches. Batch sizes are scoped at the proposal stage based on your forecast and dosage form.

How It Works

Four steps from initial enquiry to commercial production.

Tell Us About Your Product

Share your product idea, target consumer, dosage form, and any existing formulation or specification you have. We discuss claim ambitions and regulatory destination.

Formulation & Sample

If you do not have a formula, our team develops one. A sample batch is prepared for your evaluation along with a draft specification sheet.

Pilot Batch & Testing

A pilot batch is manufactured, tested in our NABL accredited laboratories for identity, assay, and microbiological limits, and placed under stability where applicable.

Commercial Production

On approval of the pilot batch, commercial manufacturing begins under GMP. Each batch is released with a certificate of analysis and supporting documentation.

Manufacturing Accreditations and Registrations

Manufacturing credentials held at our nutraceutical contract manufacturing facility.

GMP

Good Manufacturing Practices certified manufacturing facility.

AYUSH

AYUSH Manufacturing Registration for Ayurvedic and herbal products.

US FDA MoCRA

Facility registered with the US FDA under the Modernization of Cosmetics Regulation Act.

NABL accreditation applies to our analytical and testing laboratories that support this manufacturing operation, not to the manufacturing facility itself.

Export Documentation Support

Export documentation support is provided as per applicable regulatory requirements for your target market. The applicable regulatory framework and documentation scope are confirmed during proposal scoping.

Need Clinical Substantiation for Your Nutraceutical Claim?

Our CDSCO approved clinical division supports safety and efficacy claim substantiation for nutraceuticals, including bioavailability studies, efficacy trials, and Disease Risk Reduction studies under the CDSCO pathway.

Explore Clinical Trials Services

Related Services

CDMO Hub Mind to Market journey overview Formulation Development Custom R&D and product design Contract Manufacturing Personal care and Ayurvedic manufacturing Nutraceutical Testing FSSAI and AYUSH compliance testing Clinical Trials Safety and efficacy studies NABL Accredited Lab ISO/IEC 17025:2017 accredited

Frequently Asked Questions

Which licence does nutraceutical manufacturing operate under at Auriga?

Nutraceutical manufacturing at Auriga operates under our AYUSH Manufacturing Registration. FSSAI Nutraceutical Regulations apply to product-level claims and labelling on the finished product, and we support FSSAI-aligned documentation on the output. The manufacturing registration itself is AYUSH, which is the appropriate route for the Ayurvedic, herbal, and traditional knowledge nutraceutical categories we produce.

How do regulatory pathways for nutraceutical claims work?

Nutritional and efficacy claims for food supplements are handled under FSSAI guidelines. Disease Risk Reduction claims, which position the product at the food and drug boundary, require a full CDSCO clinical trial pathway. Auriga will advise on the correct pathway for your product during the initial consultation.

What dosage forms does Auriga manufacture?

Tablets (uncoated, film coated, chewable, effervescent), hard gelatin and HPMC vegetarian capsules, softgels, powder blends and sachets, granules, liquid orals such as syrups and drops, sticks, and gummies depending on scope.

What is the minimum order quantity?

Minimum order quantities depend on the dosage form and packaging. We support pilot, small commercial, and full commercial batches. Exact MOQ is agreed at the proposal stage based on your forecast and product type. Batch sizes are scalable as your brand grows.

Does Auriga support custom formulation?

Yes. Custom formulation development is available through the same group. A single relationship covers idea, formulation, testing, and commercial manufacturing, with NDA protection on all client formulations.

Can Auriga support export documentation?

Export documentation support is provided as per applicable regulatory requirements for your target market. Documentation scope and the applicable regulatory framework are confirmed during proposal scoping.

Start Nutraceutical Manufacturing

AYUSH Manufacturing Registration. GMP-certified facility. US FDA MoCRA registered. In-house testing through NABL accredited laboratories. Get a manufacturing quote within 5 business days.

+91-7428116100 Get a Manufacturing Quote