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Ambrosiya Neo Medicine Pvt. Ltd.
Index
Quality & Compliance
Document types
06
Basis
Shared with qualified buyers

Quality You Can Document

Every vitamin ingredient we supply is backed by documents your quality team can check — specifications, Certificates of Analysis, technical and safety data sheets, and composition and source statements. We publish only what current documentation supports.

Document register

06 types

  • DOC-01Certificate of Analysis · COA
  • DOC-02Product Specification
  • DOC-03Technical Data Sheet · TDS
  • DOC-04Safety Data Sheet · SDS / MSDS
  • DOC-05Composition Statement
  • DOC-06Source Statement

Shared with qualified buyers on request.

01Quality systems

A quality approach built on specifications and records

Quality is organized around documents that can be checked: what the product must be, how it is made, and the evidence that each batch meets its specification.
Stainless-steel processing vessels and pipework in a clean production area
Fig. 01Representative image
  1. 1.1

    Specification-led supply

    Each product and grade is supplied against a written specification that defines its parameters, limits and test methods.

  2. 1.2

    Qualified inputs

    Vitamin actives, carriers and packaging materials are sourced against defined requirements and supported by supplier documentation.

  3. 1.3

    Controlled processing

    Formulation and blending follow documented procedures designed for potency accuracy and batch homogeneity.

  4. 1.4

    Batch traceability

    Batch records link each lot from raw materials to dispatch, and every label and COA carries the batch identity.

  5. 1.5

    Release against specification

    Each batch is assessed against its specification before dispatch, and its results are reported on a Certificate of Analysis.

  6. 1.6

    Grade separation

    Food, nutraceutical and feed grades are specified, labelled and documented separately, so one grade is never used in place of another.

02Company & facility

Certifications & licences

Current licence and certification details are shared with qualified buyers on request. We list a licence or certification on this page only after it has been mapped to a current supporting document, together with the scope it covers — which is why no certification logos appear here.

How a credential reaches this page

  1. Step 01

    Current document on file

    The licence, permission or certificate is held in its current, valid form.

  2. Step 02

    Scope and validity checked

    The products, site and activities it covers, and its validity dates, are confirmed.

  3. Step 03

    Published with its scope

    Only then is it listed here — with the scope it actually covers, and nothing more.

03Documentation

Product documents, by grade and batch

Each document is prepared for a specific product and grade and shared with qualified buyers on request. Use the request action on any row — the enquiry form opens with the right request type.
Product document register06 rows
DOC-01Certificate of Analysis (COA)Test results for a specific batch, reported against the limits of its product specification.Per batchRequest COA
DOC-02Product SpecificationParameters, limits and test methods for the product and grade, including declared potency.Per product & gradeRequest specification
DOC-03Technical Data Sheet (TDS)Format, typical properties, handling, storage and application guidance for the grade.Per product & gradeRequest TDS
DOC-04Safety Data Sheet (SDS / MSDS)Identification, handling, storage, transport and safety information for industrial users.Per productRequest SDS
DOC-05Composition StatementThe vitamin active, carriers, excipients and any antioxidant system in the product.Per product & gradeRequest composition statement
DOC-06Source StatementThe source of the vitamin active — for example lanolin-derived or lichen-derived cholecalciferol.

Plant-Based Vitamin D3 (Lichen Source) — Manufactured for Export Markets Only. Not offered for domestic sale in India.

Per product & gradeRequest source statement

Technical support information

  • Manufacturing & process information

    An outline of how the product is made and handled, to support supplier-approval questionnaires.

    Where shareable

  • Analytical methods

    The methods used for identity, assay and other specification parameters.

    On request

  • Stability information

    Stability data for the specific grade and format, under stated storage conditions.

    Where available

Request Technical Documents

Declarations

  • Allergen declaration

    Allergen status of the product and its carriers and excipients.

    Only where supported & applicable

  • GMO declaration

    GMO status of the vitamin active and other components.

    Only where supported & applicable

  • Halal certificate or declaration

    Halal status, where a current certificate supports it for the product.

    Only where supported & applicable

  • Kosher certificate or declaration

    Kosher status, where a current certificate supports it for the product.

    Only where supported & applicable

Declarations and certificates are issued only where current documentation supports them and they apply to the specific product and grade.

Ask about a declaration

04Testing & QC

Tested against the specification, reported on the COA

Analytical chromatography instrument used for quality-control testing
Fig. 02Representative image

The parameters, limits and methods for each grade are stated on its product specification, and the results for the batch supplied are reported on its Certificate of Analysis. Where a buyer or destination market requires additional or third-party testing, it can be discussed at enquiry stage.

Typical specification parameters

Identity
Confirms that the material is the declared vitamin form.
Assay / potency
Vitamin content against the declared potency, for example in IU/g.
Appearance & physical properties
Appearance and form; for powders, particle size and flow where specified.
Loss on drying / moisture
Moisture content, where relevant to the format.
Microbiological limits
Where required by the grade and its specification.
Contaminant limits
Heavy metals and other contaminants, where required by the specification or destination market.

The exact parameters, limits and methods differ by product and grade and are stated on each specification.

05FAQ

Questions about documentation

Which documents can I request for your vitamin ingredients?

Certificates of Analysis, product specifications, technical data sheets, safety data sheets (SDS/MSDS), composition statements and source statements are prepared by product and grade. Technical support information and declarations are available where supported and applicable.

Why are no certification logos shown on this page?

We publish a licence or certification only after it has been mapped to a current supporting document, together with the scope it covers. Current licence and certification details are shared with qualified buyers on request.

Can I review a specification before a commercial discussion?

Yes. Product specifications and technical data sheets can be shared at enquiry stage so your quality team can assess suitability. A Certificate of Analysis relates to a specific batch and is issued with supply.

Are food, nutraceutical and feed grades documented separately?

Yes. Each grade has its own specification and documentation, and the grade is stated on every document. Documents for one grade are not used to support another.

What documentation is available for Plant-Based Vitamin D3 from lichen?

A specification, batch COA and source statement are prepared for international buyers. Plant-Based Vitamin D3 (lichen source) is manufactured for export markets only and is not offered for domestic sale in India.

Do you provide allergen, GMO, Halal or Kosher declarations?

Declarations and certificates such as allergen, GMO, Halal or Kosher are issued only where current documentation supports them and they are applicable to the product. Ask for the current status of the specific product and grade you need.

B2B enquiries

Qualifying ANM as a supplier? Start with the documents.

Tell us the product, grade and destination market, and which documents your quality team needs.