Eloma
01 / Method
Methodology / Process Specification

A Documented
Process.

The Eloma formulation methodology operates as a linear, non-negotiable sequence. Each step in the chain depends on the completion of the previous one. A composition without complete sourcing documentation does not proceed to ratio calibration. A batch without an independent analysis certificate does not proceed to release.

4
Process Stages
60+
Archive Entries
100%
Batches Independently Verified
7+
Documented Supplier Contracts
02 / Process Stages
01

Origin Selection

Each Eloma composition begins with an origin review. Before any ingredient enters the specification, the formulation team establishes a complete supplier profile: the geographic provenance of the raw material, the processing facility and its standard for food-grade operations, and the document trail that connects the material to its named-region origin.

Active ingredients are sourced from documented suppliers, with each batch accompanied by a certificate of composition. Sourcing prioritises suppliers whose facilities maintain food-grade processing standards. Regional sourcing is preferred where documentation standards can be verified — this preference does not mean regional exclusivity, but it does mean that alternative suppliers must meet an equivalent documentation standard before approval.

The supplier locale for each ingredient is logged in the formulation brief for that composition. This origin map — covering the primary material regions for the current range — is filed in the archive alongside the batch documentation.

World map with ingredient origin markers indicating sourcing regions for Eloma minerals and vitamins, printed documentation visible on a wooden desk
Supplier origin map — current composition cycle
Named-region documentation required for all principal ingredients
Supplier invoice and chain-of-custody record archived per batch
Alternative suppliers approved only after documentation review
02

Ratio Calibration

Once ingredient sourcing is confirmed, the formulation team sets the ratio of each component in the daily measure. This process draws on published nutritional research related to the micronutrient demands of active adult men — not on marketing-driven claims about ingredient concentration, but on the physiological logic of daily-use supplementation.

The serving composition is expressed as a fixed daily measure: a specific combination of capsule count, timing, and ingredient ratio that does not change between production cycles unless there is a documented reason grounded in ingredient availability or updated nutritional reference values. Stability in composition is a methodological principle, not a production constraint.

Each calibration decision is recorded in the formulation brief, including the reference sources consulted, the previous composition specification (if any), and the rationale for any change. This record is archived under the composition revision number.

Nutrition professional writing ingredient ratio specifications on paper at a workbench surrounded by reference documents in a clean studio environment
Ratio calibration session — composition brief ELM-24
Serving composition set per daily-measure standards and nutritional research
Formulation brief archived with reference citations and revision history
Composition stable across production cycles unless revision is documented
03

Batch Verification

Every production lot is assigned a unique batch code before it is submitted for independent analysis. The code format (ELM-YY-NN) encodes the production year and lot sequence number. This code appears on the product label and allows any customer to trace the lot through the archive.

Ingredient profiles in Eloma supplements are selected based on published nutritional research and undergo independent batch verification for quality and labelling accuracy. The analysis covers elemental concentration for each mineral constituent and active content for each vitamin component. Results are compared against the formulation brief targets. Batches that fall outside the acceptable range are not released; they are documented, retained, and subject to sourcing review.

The certificate of analysis from the independent facility is filed in the archive against the batch code. Customers who have purchased an Eloma product may request the certificate corresponding to the batch code printed on their label by contacting the team directly.

Independent laboratory technician handling Eloma supplement sample vials on a lab bench with analytical equipment visible in the background
Third-party verification visit — batch ELM-24-01
Every batch submitted to an independent laboratory before release
Certificate of analysis archived per batch code and available on request
Non-conforming batches withheld from release and logged in the archive
04

Archive Entry

Archive entry is the final stage of each production cycle. When a batch passes independent verification and receives its release status, the complete documentation package — supplier invoice, chain-of-custody record, formulation brief, and certificate of analysis — is filed under the batch code as a single archive entry.

The archive currently holds over sixty revision entries covering every production lot since 2019. Each entry is assigned a revision number that reflects both the lot sequence and any specification changes applied to that cycle. The archive format is fixed: field names, date format, revision notation, and certificate reference number are standardised across all entries.

The archive is maintained by the quality-assurance reviewer and audited annually for completeness. Any gap in the documentation sequence — a missing supplier invoice, an incomplete certificate reference — is treated as a non-conformance event and logged accordingly before the next production cycle begins.

Filing cabinet and binder system showing organised Eloma archive entries with dated tabs and batch code labels in a clean office workspace
Documentation archive — revision index, 2024
Complete documentation package filed per batch code
Archive audited annually for completeness and revision integrity
Lot records available to customers upon written request
03 / Supplier Standards

Who Eloma
Sources From.

The current Eloma range draws on seven supplier contracts covering principal mineral and vitamin materials. Each supplier was assessed against the following criteria before the first purchase order was placed: facility documentation standard, chain-of-custody capability, response time for third-party audit requests, and track record of compositional consistency across consecutive delivery batches.

Active ingredients are sourced from documented suppliers, with each batch accompanied by a certificate of composition. Sourcing prioritises suppliers whose facilities maintain food-grade processing standards. No supplier has been retained beyond a single contract cycle without re-assessment.

The origin map covering the geographic provenance of principal materials in the current composition cycle is maintained in the archive. Customers may request the current version by contacting the Eloma team.

Supplier Approval Criteria
Criterion 01
Facility Documentation

Supplier must provide full facility documentation showing food-grade processing standards applicable to the material class.

Criterion 02
Chain of Custody

Full traceability from raw material origin through processing to the delivered batch must be documentable at invoice level.

Criterion 03
Third-Party Audit Access

Supplier must support third-party audit requests within an agreed response window. Non-responsive suppliers are not renewed.

Criterion 04
Batch Consistency

Elemental profile consistency is reviewed across a minimum of three consecutive delivery batches before a supplier is confirmed for long-term engagement.

04 / Sourcing Documentation
Printed ingredient sourcing documentation spread on a table showing chain-of-custody forms and supplier certificates in a well-lit workspace
Sourcing documentation — lot record ELM-23-09
Close-up of Eloma quality-control batch containers with printed lot codes on labels arranged in rows on a clean stainless steel surface
Batch container lot codes — production run 2024
Eloma archive binder open showing completed batch verification forms with date stamps and revision numbers in neat handwriting
Archive review — annual audit session 2023

"The archive does not exist for appearances. It exists because the documentation was produced — because each step in the sourcing and verification chain generated a record that was worth keeping. The archive is a consequence of the methodology, not a feature of the marketing."

— Eloma formulation brief, introduction, revision 01-A
05 / Product Declaration
Classification

Eloma products are nutritional food-supplements registered with the applicable local regulatory authority under food-supplement classification. Products meet compositional and labelling requirements for nutritional supplement categories.

Ingredient Selection

Ingredient profiles in Eloma supplements are selected based on published nutritional research and undergo independent batch verification for quality and labelling accuracy.

Sourcing Disclosure

Active ingredients are sourced from documented suppliers, with each batch accompanied by a certificate of composition. Sourcing prioritises suppliers whose facilities maintain food-grade processing standards.

Consultation Recommendation

We recommend speaking with a qualified wellness or nutrition professional before introducing any supplement to your daily routine, particularly if you have specific dietary requirements.

06 / Questions About the Process

Methodology
FAQ.

Questions about the Eloma process — sourcing, verification, and the documentation framework.

07 / Next

Request a Lot Record.

The Eloma archive holds records for every batch produced since 2019. Contact the team with your batch code to receive the corresponding certificate of analysis.

Contact the Team