Ayurvedic · Herbal · Nutraceutical

Manufacturing Facility & Quality

Manufacturing requirements are supported through a structured facility setup for applicable Ayurvedic, Herbal and Nutraceutical products. Production, quality checks, packaging and dispatch are coordinated according to the approved product specifications and applicable requirements.

  • Production Support
  • Quality Control
  • Packaging
  • Documentation
Genuine Facility ImageAdd a clear photograph of the facility exterior or production area. Avoid stock or AI-generated factory images.
Manufacturing Location

Phase III, HSIIDC, Sector 24, Barhi, Haryana – 131101

Facility Overview

Manufacturing Support from Requirement to Dispatch

The facility setup supports applicable Ayurvedic, Herbal and Nutraceutical manufacturing requirements across production, quality control, packaging, storage and dispatch stages.

A manufacturing setup organised around the approved product requirement.

Each project begins with the product category, formulation, dosage form, quantity and packaging requirement. The applicable manufacturing route and supporting stages are then coordinated according to the reviewed specifications and required approvals.

A

Ayurvedic

Applicable Ayurvedic product and dosage-form requirements.

H

Herbal

Selected Herbal formulations and product categories.

N

Nutraceutical

Applicable Nutraceutical products across suitable formats.

  1. 01
    Production: Manufacturing against the approved product requirement and specifications.
  2. 02
    Quality Control: Applicable manufacturing and finished-product checks.
  3. 03
    Packaging: Filling, labelling and packing according to the approved presentation.
  4. 04
    Storage & Dispatch: Finished-order handling and preparation for dispatch.

Infrastructure & Production

Production Organised Around the Product Requirement

The manufacturing setup supports different operational stages required for applicable Ayurvedic, Herbal and Nutraceutical products.

Production Area ImageAdd a genuine, clear photograph showing the relevant production area. Avoid stock or AI-generated machinery images.
Manufacturing Infrastructure

Production Overview

Each product follows its reviewed manufacturing route.

The product category, formulation, dosage form, specifications and order requirement are reviewed before production begins. Manufacturing then proceeds according to the approved requirement and applicable process.

Requirement ReviewProduct category, formulation and dosage form.
ProductionManufacturing against the approved specifications.
Quality ChecksApplicable checks during and after manufacturing.
Pack PreparationFilling and packaging against the approved presentation.

The exact production setup and process depend on the selected product, formulation, dosage form and applicable manufacturing requirements.

Manufacturing Formats

Multiple Dosage Forms

Manufacturing support is available for applicable products across the following formats, subject to product-specific review and feasibility.

  • Tablets
  • Capsules
  • Softgel Capsules
  • Syrups & Liquids
  • Powders & Sachets
  • Drops
  • Effervescent Tablets
  • Hair Oil & Pain Oil
  • Selected Hair Care
  • Selected Skin Care

Quality Control

Quality Checks Aligned with the Approved Requirement

Quality is considered throughout the manufacturing process—from reviewing the product specifications to production, packaging and finished-order verification.

Quality Across the Process

Checks begin before manufacturing starts.

Product category, formulation, dosage form, specifications and packaging requirements are reviewed before the requirement is released for manufacturing.

  1. 01
    Product requirement and category review
  2. 02
    Specifications and manufacturing inputs
  3. 03
    Production-stage checks, as applicable
  4. 04
    Finished-product and packaging verification

The exact quality parameters and checks depend on the individual product, category and approved specifications.

01

Product & Specification Review

The product type, formulation, dosage form and relevant specifications are reviewed before manufacturing proceeds.

02

Manufacturing-Stage Checks

Applicable checks are considered during production according to the selected product and manufacturing requirement.

03

Finished-Product Review

Finished-product requirements are checked against the approved specifications and applicable quality parameters.

04

Packaging & Label Verification

Pack presentation, approved artwork and relevant batch details are reviewed before the order moves towards dispatch.

Quality requirements are product-specific. Applicable checks, documents and parameters are discussed according to the selected product category and manufacturing requirement.

Formulation Support

Start with a Formulation, Reference or Product Idea

You do not need the same level of product information at the first discussion. Share what is currently available and the requirement can be reviewed accordingly.

01

Your Own Formulation

Share the proposed composition, ingredient details, dosage form, specifications and intended product category for a manufacturing-feasibility review.

02

A Reference Product

Send the available label, product photograph, composition or specifications so the intended formulation and packaging requirement can be understood.

03

A Product Idea

Tell us the product category and format you are planning. Applicable formulation and manufacturing options can then be discussed.

Requirement Evaluation

How the product requirement moves forward

The shared information is considered against the selected category, intended dosage form and applicable manufacturing requirements before commercial details are confirmed.

  1. 01
    Product category and intended use
  2. 02
    Formulation, ingredients or reference
  3. 03
    Dosage form and specifications
  4. 04
    Manufacturing feasibility and requirements
  5. 05
    Quantity, packaging and presentation
  6. 06
    MOQ, commercial discussion and quotation

Packaging & Order Handling

From Approved Packaging to Final Dispatch

Packaging, finished-order handling and dispatch preparation are coordinated according to the approved product presentation and commercial requirement.

Packaging or Dispatch ImageAdd a genuine photograph showing product packing, finished packs or dispatch-ready cartons.
Finished Product Preparation

Packaging Coordination

Product and packaging details are finalised together.

The product container, fill or pack quantity, label, outer carton and final presentation are discussed according to the selected product and order requirement.

  • Container, bottle, jar, strip or applicable pack format
  • Fill quantity, serving quantity or unit configuration
  • Label and outer-carton requirements
  • Approved artwork and mandatory product information
  • Final pack presentation and order identification

Packaging options and material availability vary according to the product, format, order quantity and approved requirement.

01

Packaging

Filling, labelling and outer packaging proceed according to the approved product specifications and final artwork.

02

Finished-Order Handling

The completed order is organised with the relevant product and order details before dispatch preparation.

03

Dispatch Coordination

Final quantity, batch-related details, payment and dispatch information are coordinated before the order is released.

Certifications & Documentation

Verified Documents, Displayed with Clear Scope

Certification and licence details should be read according to their stated scope, validity, applicable facility and relevant product category.

GMPCertificate Image

GMP Certificate

Supports applicable Good Manufacturing Practice requirements within the scope stated on the verified certificate.

  • Certificate No.Add from document
  • ValidityAdd from document
  • ScopeAdd from document
Certificate file to be added
ISOCertificate Image

ISO Certification

Forms part of the documented quality-management framework within the scope stated on the verified certificate.

  • Certificate No.Add from document
  • ValidityAdd from document
  • ScopeAdd from document
Certificate file to be added
FSSAILicence / Registration

FSSAI Licence

Relevant to applicable food and Nutraceutical product requirements within the category and scope stated on the document.

  • Licence No.Add from document
  • ValidityAdd from document
  • CategoryAdd from document
Document file to be added
QMCVerified Document

QMC Document

Document title, issuing authority and applicable scope will be displayed exactly as stated on the verified copy.

  • Document No.Add from document
  • ValidityAdd from document
  • ScopeAdd from document
Document file to be added

Product & Order Documentation

Documentation discussed according to the requirement

The documents applicable to a manufacturing project depend on the selected product, category, specifications and agreed order process.

  • Product and composition details
  • Approved artwork information
  • Packaging specifications
  • Manufacturing-related details
  • Applicable quality documents
  • Final order and dispatch information

Frequently Asked Questions

Facility & Quality Questions, Answered

Quick answers about the manufacturing location, product formats, quality process, certifications, documentation and facility visits.

Where is the manufacturing facility located?

The manufacturing location is Phase III, HSIIDC, Sector 24, Barhi, Haryana – 131101.

Which product categories are supported?

Applicable Ayurvedic, Herbal and Nutraceutical product requirements can be discussed. Every product is reviewed according to its category, formulation, dosage form and applicable requirements.

Which dosage forms can be manufactured?

Applicable requirements may include tablets, capsules, softgels, syrups and liquids, powders and sachets, drops, effervescent tablets, Hair Oil, Pain Oil and selected personal-care formats.

Is third-party and private label manufacturing available?

Yes. Applicable third-party and private label manufacturing requirements can be discussed according to the selected product, specifications, quantity and packaging requirement.

Can I share my own formulation or a reference product?

Yes. You may share your formulation, composition, reference label, product photograph or initial product idea for requirement and feasibility review.

How is quality considered during manufacturing?

Quality is considered through product and specification review, applicable manufacturing-stage checks, finished-product review and packaging verification according to the approved requirement.

Which certifications and licences are available?

Verified GMP, ISO, FSSAI and other applicable documents can be reviewed according to their stated scope, validity, facility and relevant product category.

Does every approval apply to every product?

No. The applicability of a licence, certification, approval or supporting document depends on the individual product category and its regulatory requirements.

Can I request documents for my product requirement?

Yes. Share the product category, product name and dosage form. The relevant available documents can then be discussed according to the requirement.

Can clients visit the manufacturing facility?

A facility visit can be discussed after the company and product requirement are shared. Visits are subject to prior appointment and final visit confirmation.

Still have a facility or quality question?

Share your product category, dosage form and requirement for a relevant discussion.

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Start Your Manufacturing Enquiry

Planning an Ayurvedic or Nutraceutical Product?

Share your product requirement with WIN Formulation. The category, formulation or reference, dosage form, quantity and packaging requirement will be reviewed before the applicable manufacturing and commercial details are discussed.

  • Product Category
  • Product Name
  • Formulation or Reference
  • Dosage Form
  • Approximate Quantity
  • Packaging Requirement