GMP Certified · AYUSH Manufacturing Registration · US FDA MoCRA

Contract Manufacturing India: GMP Certified Facility

Auriga Research provides contract manufacturing for personal care, nutraceutical, and herbal products at our GMP-certified facility in Baddi, Himachal Pradesh.

The facility holds AYUSH Manufacturing Registration for Ayurvedic and herbal scopes, and is registered with the US FDA under the Modernization of Cosmetics Regulation Act (MoCRA). Brand owners can supply finished formulations or work with our team to develop and stabilise a new product before production.

Documentation, batch records, and finished product release are managed under documented GMP procedures. Manufacturing is supported by our NABL-accredited testing laboratories under the same group, which conduct raw material, in-process, stability, and release testing.

Manufacturing Facility, Baddi, Himachal Pradesh

Our contract manufacturing facility is located in Baddi, Himachal Pradesh. The facility is GMP certified, holds AYUSH Manufacturing Registration, and is registered with the US FDA under MoCRA.

Auriga contract manufacturing facility exterior, Baddi, Himachal Pradesh
GMP Manufacturing Facility
Baddi, Himachal Pradesh
Auriga contract manufacturing facility interior, processing area
Processing area
Auriga contract manufacturing facility, filling and packaging line
Filling and packaging line

Manufacturing Equipment

Confirmed production assets at the Baddi facility. Run size is confirmed by your SPOC at quote stage.

KOTHARI PRECIKOT Liquid Manufacturing Vessel 2000L

Liquid manufacturing

High-shear and vacuum emulsification homogeniser used for creams, lotions, serums, and emulsions. 2,000-litre working capacity.

Ointment Manufacturing Vessel 500 Kg

Semi-solid manufacturing

Jacketed steam-heated vessel for ointments, balms, pastes, and high-viscosity semi-solid formulations.

PacMac Double Head Filling Machine with Smart Fill Technology

Liquid filling line

Automatic double-head filling line for bottles and containers, supporting a wide range of fill volumes and viscosities.

ACG PAMPAC VP-120 Auto Cartonator

Automatic cartoning

Vertical pick-and-place cartonator with leaflet insertion and batch coding integration.

Reverse Osmosis and SS Loop Water Purification System

Pharma-grade water system

RO with stainless-steel circulating loop feeding production with pharma-grade purified water, with continuous TDS, conductivity, and microbial monitoring.

Dosage Forms and Packaging

Liquid, semi-solid, and solid dosage forms across the four primary packaging formats used by personal care, nutraceutical, and herbal brands.

Liquids

Shampoos, conditioners, hair oils, face washes, toners, body washes, serums.

Semi-solids

Creams, ointments, gels, lotions, balms, pastes.

Solids

Powders, granules, sachet powders, bath salts.

Packaging Formats

TubesJarsBottlesSachets

Stability Chambers

Walk-in and reach-in stability chambers operating across multiple temperature and humidity conditions, available to support batch and development-scale stability programmes.

Walk-in Chambers

Large-volume stability chambers for batch-scale stability studies and reserve sample storage.

Reach-in Chambers

Multiple reach-in chambers used for smaller batch and development-scale stability programmes.

Operating Conditions

40 °C
75 % RH
25 °C
60 % RH
30 °C
75 % RH
50 °C
60 % RH
60 °C
60 % RH

Product Categories Covered

Three product categories supported at the contract manufacturing facility.

Personal Care

Skincare, sunscreens, haircare, body care, men's grooming, baby care, and sensitive-skin formulations.

Nutraceuticals

Tablets, capsules, softgels, powders, sachets, and liquid nutraceuticals, manufactured under AYUSH Manufacturing Registration.

Herbal & AYUSH

Classical and proprietary Ayurvedic formulations, herbal cosmetics, and herbal supplements.

Who Engages Auriga for Contract Manufacturing

Seven buyer profiles use our contract manufacturing service, from D2C founders to export-focused brands.

Brands Requiring GMP-Certified Third-Party Manufacturing

Brand owners that need a GMP-certified manufacturing partner with documented batch records and audit-ready quality systems.

D2C Founders Scaling from Prototype to Commercial

Direct-to-consumer founders moving from a working prototype to commercial production and looking for a manufacturing partner with pilot to commercial scale-up.

Nutraceutical Companies Requiring AYUSH Manufacturing

Nutraceutical brands manufacturing Ayurvedic, herbal, and traditional-knowledge supplements that require AYUSH Manufacturing Registration.

Pharma Companies Expanding into Personal Care or Wellness

Pharmaceutical companies extending into personal care, nutraceutical, or wellness categories and looking for a partner familiar with pharma quality standards.

Private Label Businesses

Retailers, distributors, and aggregators developing their own private label ranges in personal care and wellness.

Retail Chains

Pharmacy, beauty, supermarket, and specialty retail chains building in-house brands across personal care and wellness categories.

Export Brands Requiring MoCRA Documentation

Export-focused brands selling cosmetics into the US market and needing manufacturing partners registered with the US FDA under MoCRA.

Why Auriga for Contract Manufacturing

Six reasons brands choose Auriga as their contract manufacturing partner.

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.

AYUSH Manufacturing Registration

AYUSH Manufacturing Registration is in place for the contract manufacture of Ayurvedic and herbal formulations alongside personal care and nutraceutical scopes.

US FDA MoCRA Registered

The facility is registered with the US FDA under the Modernization of Cosmetics Regulation Act, supporting brands with cosmetic products in the US distribution scope.

In-House Testing via NABL Laboratories

Manufacturing is supported by 5 NABL-accredited testing laboratories under the same group. Raw material, in-process, stability, and release testing run alongside production. NABL accreditation applies to the testing laboratories and not to the manufacturing facility.

Integrated Formulation and Clinical Studies

Formulation development and CDSCO-approved clinical studies are available through the same group, so brands can scope these services alongside manufacturing.

Low MOQ, Flexible Batch Sizes

We support pilot, small commercial, and full commercial batches. Run size is confirmed by your SPOC at quote stage based on your forecast and dosage form.

How It Works

Four steps from initial enquiry to finished goods delivery.

01

Share Your Product Brief

Share your product brief with the SPOC, who confirms feasibility and run size.

02

Formulation & Stability

Formulation and stability data are submitted by you or developed in-house before production begins.

03

Manufacturing & QC

Manufacturing runs at our GMP facility with in-process quality checks and complete batch documentation.

04

Release & Delivery

Release testing and batch documentation are delivered with the finished goods.

Manufacturing Accreditations and Registrations

Manufacturing credentials held at the Baddi facility.

GMP logo
GMP

Good Manufacturing Practices certified manufacturing facility.

AYUSH logo
AYUSH

AYUSH Manufacturing Registration for Ayurvedic and herbal products.

US FDA MoCRA logo
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.

Frequently Asked Questions

What dosage forms can Auriga manufacture on contract?
Auriga manufactures liquid, semi-solid, and solid formulations at our GMP facility in Baddi, Himachal Pradesh. Liquids include shampoos, conditioners, hair oils, face washes, toners, body washes, and serums. Semi-solids include creams, ointments, gels, lotions, balms, and pastes. Solids include powders, granules, sachet powders, and bath salts. Packaging formats include tubes, jars, bottles, and sachets.
Where is the manufacturing facility located and what accreditations does it hold?
The manufacturing facility is located in Baddi, Himachal Pradesh, one of India's primary pharmaceutical and personal care manufacturing locations. The facility is GMP certified, holds AYUSH Manufacturing Registration, and is registered with the US FDA under MoCRA. NABL accreditation applies to our analytical and testing laboratories that support this manufacturing operation, not to the manufacturing facility itself.
What is the production capacity?
Run size is confirmed by your SPOC at quote stage based on your forecast, dosage form, and packaging requirements. The facility supports pilot, small commercial, and full commercial batches. Equipment includes a Kothari Precikot Liquid Manufacturing Vessel 2000L, a 500 Kg Ointment Manufacturing Vessel, a PacMac Double Head Filling Machine with Smart Fill Technology, an ACG PAMPAC VP-120 Auto Cartonator, and a Reverse Osmosis and SS Loop water purification system.
What stability chamber conditions are supported?
Walk-in and reach-in stability chambers support multiple conditions including 40 °C / 75 % RH, 25 °C / 60 % RH, 30 °C / 75 % RH, 50 °C / 60 % RH, and 60 °C / 60 % RH. Stability studies are run for accelerated and long-term programmes as required by your shelf-life target and regulatory destination.
Does Auriga support Ayurvedic and herbal contract manufacturing?
Yes. AYUSH Manufacturing Registration is in place at the Baddi facility for the contract manufacture of classical and proprietary Ayurvedic formulations, herbal cosmetics, and herbal supplements.
Can I supply my own formula for contract manufacturing?
Yes. We accept client-supplied formulations under NDA. Our team reviews the formula for manufacturability, conducts a pilot batch to confirm process parameters, and performs stability testing before scaling to commercial production. Where modifications are needed for stability or processability, we recommend adjustments and seek your approval before proceeding.
Do you provide export documentation?
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.

Start Contract Manufacturing in Baddi

GMP certified. AYUSH Manufacturing Registration. US FDA MoCRA registered. Get a manufacturing quote within 5 business days.

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