Cosmetic and herbal third-party manufacturing
enquiry@gayatriherbalsindia.com +91 98675 40449 Manufacturing excellence in India
Zero-Compromise Standards

Quality Built Into Every Stage of Manufacturing

At Gayatri Herbals Pvt. Ltd., quality is integrated throughout the manufacturing process—from incoming raw-material inspection and formulation development to in-process checks, filling, packaging and finished-product evaluation. Established in 1996, our manufacturing approach combines documented processes, trained personnel, modern production infrastructure and established quality systems to support consistency across herbal, cosmetic, personal care, Ayurvedic and wellness products. gayatri herbals information

Accreditations & Standards

Manufacturing Guided by Established Quality Practices

GMP

Good Manufacturing Practice

Established Good Manufacturing Practices help guide manufacturing processes, documentation, operational controls and product-quality procedures.

AYUSH

Defined Quality Specifications

Raw materials and finished products are evaluated against defined specifications relevant to the particular formulation and product.

ISO

Quality Management Standards

The supplied company information states that Gayatri Herbals' manufacturing operations have been associated with ISO quality standards, including ISO 9001. gayatri herbals information

EXPORT

International Market Requirements

Products are supplied to markets including Canada, Australia, Europe and the Gulf region, requiring applicable quality, documentation and regulatory requirements to be considered for the respective markets. gayatri herbals information.

Facility Architecture

Plant Zones & Production Capabilities

Our manufacturing unit is physically segregated into distinct environmental zones to eliminate cross-contamination and ensure repeatable batch consistency.

01

Compounding & Formulation Suites

Equipped with SS 316-grade mixing vessels with high-shear homogenizers, jacketed heating/cooling, and planetary mixers capable of processing cold creams, serums, shampoos, and heavy herbal pastes.

  • Batch capacities from 50 kg to 2,000 kg
  • Positive pressure HEPA air circulation
  • Closed-loop sanitary fluid transfer
02

Automated Cleanroom Filling Lines

Precision volumetric piston fillers, automatic multi-head rotary fillers, ultrasonic tube crimping, induction cap sealers, and laser batch coders.

  • Bottles, jars, tubes, vials, and sachets
  • Automated check-weighing on all units
  • UV de-dusting before filling
03

Analytical & Microbial QA Lab

Equipped with calibrated instrumentation for wet chemistry, pH, viscosity, refractive index, density, and a separate bio-safety microbiological testing chamber.

  • In-house Total Viable Count (TVC) testing
  • Brookfield rotational viscometer
  • Accelerated stability chambers (45°C / 75% RH)
04

Quarantine & Controlled Storage

Spacious, humidity-monitored warehouse with distinct status demarcations (Quarantine, Under Test, Approved, and Rejected) for raw ingredients and finished goods.

  • Temperature-sensitive botanical storage
  • Complete FIFO / FEFO inventory system
  • Barcode-linked pallet dispatch
Analytical Rigor

Batch Testing Protocols & Release Criteria

No finished product leaves our facility without passing our comprehensive three-tier testing matrix.

Testing Domain Specific Parameters Evaluation Method Quality Standard
Physicochemical pH Balance, Viscosity, Specific Gravity Digital pH Meter, Brookfield Viscometer, Pycnometer Target range ± 0.3 pH; ± 10% target cP
Sensory & Organoleptic Color, Texture, Scent Profile, Skin Absorption Double-blind sensory panel vs. Master Standard 100% concordance with benchmark retain
Microbiological Safety Total Aerobic Microbial Count, Yeast & Mold Plate Count Method (USP / IS standard) < 100 CFU/g (cosmetic standard compliance)
Pathogen Screening E. coli, S. aureus, P. aeruginosa, Salmonella Selective culture media plating Completely Absent in 1g / 1mL
Thermal Stability Oven challenge (45°C @ 75% RH for 90 days), Freeze-Thaw 3x Temperature shock cycling Zero phase separation, cracking, or odor drift
Container Compatibility Stress crack resistance, pump stroke volume, leakage Vacuum chamber leak test (-0.5 bar) Zero product seepage or container degradation
Full Traceability

Complete Batch Manufacturing Records (BMR)

Every single batch is documented from raw herb cultivation lot to finished pallet dispatch. We retain retention samples and complete batch records for a minimum of 3 years to ensure absolute post-market brand security.

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