GMP Certified · FSSAI Compliant · NABL Tested

Nutraceuticals Contract Manufacturing India | GMP Certified

Auriga Research provides GMP-certified nutraceuticals contract manufacturing in India for health supplement brands, pharmaceutical companies, and Ayurvedic product manufacturers. We manufacture tablets, capsules, powders, liquids, and granules with complete formulation development, quality testing, and regulatory documentation.

Our manufacturing facility processes vitamins, minerals, herbal extracts, amino acids, probiotics, and proprietary nutrient blends under documented GMP procedures. Every batch undergoes full analytical testing in our NABL-accredited laboratory — identity, assay, dissolution, disintegration, heavy metals, pesticide residues, aflatoxins, and microbiological limits.

All nutraceutical products manufactured at Auriga Research comply with FSSAI regulations for health supplements and nutraceuticals. We also prepare documentation for AYUSH product registrations and export compliance for international markets.

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Manufacturing Capabilities

GMP

Certified manufacturing facility with documented batch records

FSSAI

Compliant with health supplements and nutraceuticals regulations

NABL

In-house accredited lab for complete quality testing

R&D

Custom formulation development and stability studies

Dosage Forms

Multiple dosage form capabilities for vitamins, minerals, herbal extracts, and proprietary blends.

Tablets

Uncoated, film-coated, chewable, and effervescent tablets. Granulation, compression, and coating with full dissolution and disintegration testing.

Capsules

Hard gelatin and HPMC vegetarian capsules. Powder, pellet, and granule fills with accurate weight control and content uniformity.

Powders & Sachets

Powder blends, instant-mix sachets, and granulated preparations. Homogeneous mixing with content uniformity testing per pharmacopoeial standards.

Liquid Preparations

Syrups, suspensions, oral drops, and liquid supplements. Accurate compounding, filling, and microbiological testing for shelf life assurance.

Herbal & Ayurvedic

Herbal extract processing, standardised extracts, churnas, and traditional formulations. AYUSH compliance documentation and marker compound testing.

Probiotics

Probiotic capsules and sachets with controlled storage and handling. CFU enumeration, strain identity verification, and stability under storage conditions.

Quality Testing & Compliance

Analytical Testing

✓ Identity and assay (HPLC, GC, UV-Vis)
✓ Dissolution and disintegration testing
✓ Heavy metals (Pb, Cd, As, Hg) by ICP-MS
✓ Pesticide residue analysis
✓ Aflatoxin testing (B1, B2, G1, G2)

Regulatory Compliance

✓ FSSAI health supplements regulations
✓ AYUSH product registration support
✓ Stability studies (ICH-aligned)
✓ Microbiological limits testing
✓ Label claim verification

Related Services

Formulation Development Custom R&D and product design Personal Care Manufacturing Cosmetics and skincare Nutraceutical Testing FSSAI, AYUSH compliance testing FSSAI Approved Lab Food safety testing AYUSH Testing Herbal and traditional medicine NABL Accredited Lab ISO/IEC 17025:2017

Frequently Asked Questions

What nutraceutical dosage forms does Auriga Research manufacture?

Auriga Research manufactures tablets (uncoated, film-coated, chewable, effervescent), hard gelatin capsules, soft gelatin capsules, powder blends and sachets, granules, liquid orals (syrups, suspensions, drops), and gummies. Our GMP-certified facility handles herbal extracts, vitamins, minerals, amino acids, probiotics, and proprietary blends with documented batch manufacturing records and complete traceability.

Is the nutraceuticals manufacturing facility FSSAI compliant?

Yes. Our nutraceuticals manufacturing operations comply with FSSAI (Food Safety and Standards Authority of India) regulations. Products are manufactured per FSSAI licensing requirements, and all finished products are tested for compliance with the Food Safety and Standards (Health Supplements, Nutraceuticals, Food for Special Dietary Use, Food for Special Medical Purpose, Functional Food and Novel Food) Regulations, 2016. Our NABL-accredited lab performs the complete analytical testing required for FSSAI compliance.

What is the MOQ for nutraceutical contract manufacturing?

Minimum order quantities for nutraceuticals depend on the dosage form. For tablets and capsules, MOQs typically start at 50,000 units per batch. For powder sachets, MOQs start at 10,000 sachets. Liquid preparations start at 500 litres. Pilot batches for formulation approval are available at lower quantities. We work with both emerging supplement brands and established nutraceutical companies.

Start Nutraceutical Manufacturing

GMP-certified contract manufacturing for tablets, capsules, powders, and liquids. FSSAI compliant with NABL-accredited quality testing. Get a quote within 5 business days.

+91-7428116100 Get a Manufacturing Quote