Iralenov
METHODOLOGY — DOC.V04 / 2026

Standards.
Process.
Record.

The Iralenov methodology documents how formulations are assembled — from initial ingredient research through to independent batch analysis. This page describes the five-stage sequence in full.

7
Formulations
5
Process Stages
100%
Independently Verified
THE FIVE-STAGE FORMULATION PROCESS
01
RESEARCH REVIEW

Published-Research Intake

Each formulation begins with a structured review of published nutritional research. Sources include peer-reviewed journals, EU nutrition reference databases, and systematic reviews compiled by qualified nutrition professionals. The review identifies candidate ingredients with documented roles in supporting specific aspects of active male health — energy metabolism, muscle function, immune support, and antioxidant defence.

REFERENCE STANDARDS
  • —EFSA NDA Panel nutrient reference values
  • —EU Regulation 432/2012 authorised health claims
  • —PubMed / Cochrane systematic review library
  • —Belgian Federal Agency for the Safety of Food Chain (FASFC) guidelines
Research documents and nutritional reference papers spread across a clean desk under studio lighting, with annotation notes
02
INGREDIENT SELECTION

Composition Architecture

Selected ingredients are assessed for form (bioavailability profile), quantity (alignment to EU reference intake levels), and compatibility. Ingredient forms are selected for absorption characteristics — for example, magnesium glycinate over oxide, methylcobalamin over cyanocobalamin. The final composition is documented as a specification sheet before supplier engagement.

SELECTION CRITERIA
  • —Absorption form preferred over raw elemental
  • —Quantities set to complement typical dietary intake
  • —Plant-derived or food-grade sources where available
  • —No artificial fillers, synthetic colours, or fragrance agents
  • —Allergen declaration reviewed at specification stage
03
SUPPLIER ENGAGEMENT

Sourcing Verification

Active ingredients are sourced from documented European and Scandinavian suppliers with verifiable supply chains. Each supplier provides a certificate of analysis per ingredient lot, documenting active compound concentration and absence of contaminants. Iralenov maintains a supplier register updated per production cycle.

SUPPLIER REQUIREMENTS
  • —Certificate of analysis per ingredient lot
  • —Food-grade processing facility documentation
  • —Chain-of-custody traceability from source material
  • —Heavy-metal and pesticide screening per lot
  • —Annual re-audit of documentation currency
Supplier documentation and ingredient certificates laid on a clean workspace surface, overhead lighting, stamps visible
04
PRODUCTION & BATCH CODING

Manufacturing Record

Production takes place at a food-grade manufacturing facility operating under EU food supplement production standards. Each production run is assigned a unique batch code (format: Q[QUARTER]-[YEAR]-IRA[REF]) which links the finished product to the specification sheet, ingredient lot certificates, and subsequent verification results. Batch codes are printed on base labels.

PRODUCTION STANDARDS
  • —Batch coding: Q[Q]-[YY]-IRA[REF] format
  • —Temperature-controlled storage during production
  • —In-process weight checks per fill run
  • —Sealed batch-retention samples held 36 months
  • —Production log filed per batch before dispatch
05
INDEPENDENT VERIFICATION

Third-Party Analysis

Each finalised batch is submitted to an independent, accredited analytical laboratory before being made available. Analysis confirms declared ingredient concentrations, checks for microbiological contamination, and verifies heavy-metal absence. Results are reconciled against the production specification. Any batch where results fall outside declared tolerances is withheld and reviewed.

ANALYSIS SCOPE
  • —ICP-MS elemental analysis (minerals, heavy metals)
  • —HPLC quantification (active botanical compounds)
  • —Microbiological panel (total viable count, yeast, mould)
  • —Oxidation index for lipid-based formulations
  • —Label compliance cross-check per EU Reg. 1169/2011
Independent laboratory verification bench with batch-coded sample containers and analysis equipment under bright studio lighting
SUPPLIER GEOGRAPHY — 2026 REGISTER

Where Ingredients Originate

Iralenov's ingredient register draws from eight documented supplier relationships across Northern and Western Europe. The geographic distribution reflects a deliberate preference for proximity — shorter logistics chains reduce exposure variability and allow faster documentation retrieval for audit purposes.

Each supplier relationship undergoes annual documentation review. Supplier status (active / under review / substituted) is recorded in the internal register. No ingredient is sourced from an unverified supplier. If documentation cannot be produced within five working days of request, the supplier is placed under review and alternative sourcing is identified.

NETHERLANDS — SUPPLIER NL-04
Magnesium & zinc mineral salts. Chelated forms.
ACTIVE
FRANCE — SUPPLIER FR-11
Organic pea protein isolate. Yellow pea cultivation.
ACTIVE
NORWAY — SUPPLIER NO-07
Cold-water marine oil concentrate. Anchovy & sardine origin.
ACTIVE
INDIA — SUPPLIER IN-02
KSM-66 ashwagandha root extract. Standardised 5% withanolides.
ACTIVE
SWEDEN — SUPPLIER SE-09
Rhodiola rosea root. Standardised 3% rosavins.
ACTIVE
GERMANY — SUPPLIER DE-06
Ubiquinol CoQ10 in oil-suspension format. Kaneka Q10 supply chain.
ACTIVE
BELGIUM — SUPPLIER BE-01
Encapsulation and final assembly. EU food supplement standards.
ACTIVE
EU CERTIFIED — SUPPLIER EU-03
Hemp seed oil and whole seed protein. EU-certified non-GMO growers.
ACTIVE
TRANSPARENCY RECORD
LABELLING ACCURACY

What Is Declared Is What Is Present

Declared ingredient quantities on Iralenov labels reflect actual batch composition confirmed via independent analysis. Tolerances are maintained within ±10% of declared value. Where a batch falls outside this window, labelling is corrected before dispatch or the batch is withheld.

NO UNDISCLOSED ADDITIONS

Complete Ingredient Disclosure

Iralenov formulations contain no undisclosed excipients. Every ingredient in the final product — including encapsulation materials, anti-caking agents, and coating — appears on the product label. Excipient quantities are not required under EU labelling law but are provided on request.

DOCUMENT ACCESS

Batch Records on Request

Third-party laboratory results and supplier certificates of analysis are available upon written request. Requests should reference the batch code (printed on product base) and the specific formulation reference number. Iralenov responds within two working days.

REGULATORY FRAMEWORK

Belgian & EU Context

Iralenov food supplements are formulated and labelled in accordance with applicable EU and Belgian food supplement regulations. This includes EU Directive 2002/46/EC on food supplements, EU Regulation 1169/2011 on food information, and Belgian Royal Decree of 28 July 2017 on food supplements.

Authorised health claims used in Iralenov content are drawn exclusively from the EU Register of authorised nutrition and health claims (EU Reg. 432/2012 and subsequent amendments). No claims are made that are not listed on the EU Register as authorised.

Iralenov is an independent wellness resource focused on everyday nutrition and active lifestyle practices for men. The content is not affiliated with any governmental or institutional body.

Brussels editorial workspace with regulatory documentation and ingredient specification sheets on a clean surface
BRUSSELS OFFICE — REGULATORY FILES / 2026
KEY REGULATORY REFERENCES
  • EU Directive 2002/46/EC — Food supplements
  • EU Regulation 432/2012 — Authorised health claims
  • EU Regulation 1169/2011 — Food information
  • Belgian Royal Decree 28 July 2017 — Supplements
  • FASFC Guidelines — Belgian Food Safety Authority
QUALITY STANDARDS SUMMARY
7
Active formulations in catalogue
8
Documented supplier relationships
±10%
Labelling tolerance window
36mo
Batch sample retention period
EDITORIAL NOTE

Ingredient profiles in Iralenov supplements are selected based on published nutritional research and undergo independent batch verification for quality and labelling accuracy. 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. Iralenov content does not constitute individual nutritional advice.