Source.Verify.Release.
The Oranevel methodology is the set of documented procedures that governs how each supplement formulation moves from ingredient sourcing through composition calibration to independent verification and final release. Every step produces a written record. Every record is retained.
The Six-Stage Process
Ingredient Sourcing & Supplier Qualification
Each ingredient passes through a documented supplier qualification process before entering the production chain. The qualification checklist covers: food-grade processing facility status, chain-of-custody documentation, and certificate of composition from the previous production run. Suppliers who cannot provide full documentation are not onboarded regardless of price.
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.
- Supplier qualification checklist
- Certificate of composition
- Cold-chain transit log
- Origin map entry
Composition Calibration & Ratio Setting
Before production begins, the ingredient ratio is calibrated against the target formulation specification. This calibration step verifies that incoming ingredient concentrations are consistent with prior batches. Deviations above ±2% from the target elemental amount trigger a recalibration hold before production proceeds.
The calibration record captures the measured concentration of each ingredient, the target amount, the deviation percentage, and the sign-off from the lead nutrition professional.
- Ingredient ratio table
- Calibration deviation log
- Production go/no-go record
Production & Batch Coding
Production at the Jakarta facility follows a food-grade encapsulation process. Each production run produces a finite batch with a unique lot code. The lot code is printed on every container and links to the complete batch record in the archive. No batch is dispatched without a valid lot code assigned.
Lot codes follow the format: [INGREDIENT-CODE]-[YEAR]-[BATCH-NUMBER]. The lot record for each code includes: production date, facility shift record, ingredient lot numbers, and the name of the production supervisor.
- Lot code assignment record
- Production shift log
- Batch size record
Independent Batch Verification
A sample from each batch is submitted to an independent laboratory — not affiliated with Oranevel — for elemental composition analysis. The laboratory confirms that the measured ingredient concentrations match the stated label values within an acceptable tolerance. Results are returned as a formal report referencing the lot code.
Ingredient profiles in Oranevel supplements are selected based on published nutritional research and undergo independent batch verification for quality and labelling accuracy. A batch that fails verification is held from release and the deviation is documented in the corrective action log.
- Independent lab report
- Elemental analysis table
- Pass/hold decision record
- Corrective action log (if applicable)
Release Authorisation & Labelling
A batch is authorised for release only after the independent verification report has been received, reviewed, and signed off. The release authorisation record contains: the lot code, the date of independent verification, the laboratory name, the verification outcome, and the authorising specialist's name.
Final labelling is completed after release authorisation. All labels display the lot code, the production date, the best-before date, and the full elemental composition as verified in Step 04.
- Release authorisation form
- Final label proof
- Dispatch manifest
Lot Record Archive & Retention
All documents produced in steps 01 through 05 are archived under the lot code. The archive entry is dated and assigned a revision number. The archive is maintained in the Jakarta facility and backed up to an off-site location. Retention period: minimum five years from the production date.
Registered correspondents may request access to lot records for specific batches by referencing the lot code from the product label. Requests are processed within five working days.
- Complete lot record file
- Archive entry revision log
- Off-site backup confirmation
Supplier Standards
Jakarta, 2024 — The supplier qualification standard was revised to its current form (revision 05-B) following the facility expansion. The revision added a requirement for in-transit temperature logging on all shipments of moisture-sensitive ingredients, including zinc and selenium forms.
Suppliers are assessed on an annual cycle. The assessment covers: facility status, prior-year certificate accuracy (compared against independent results), on-time delivery record, and chain-of-custody documentation quality. Suppliers who score below the threshold on any of the first two criteria are placed on review hold.
The origin map maintained in the archive records the geographic source region for each active ingredient across all production runs. Named-region material is preferred where the regional sourcing origin is relevant to the ingredient's elemental profile.
All supplier facilities must demonstrate and maintain food-grade processing status as a prerequisite. Status is verified annually against the relevant regulatory framework for the supplier's operating country.
Each delivery is accompanied by a full chain-of-custody document tracing the ingredient from the point of origin through processing to the delivery point. Incomplete documentation triggers a receipt hold.
Moisture-sensitive ingredients — including zinc bisglycinate, selenomethionine, and methylcobalamin — are transported under cold-chain conditions. Temperature logs accompany each shipment and are retained in the ingredient receipt record.
Ingredient Origin Map
Zinc Bisglycinate
Sourced from a documented supplier operating in the Southeast Asian region. Certificate of composition included with each delivery. Annual audit cycle active.
Magnesium Glycinate
Regional supplier; cold-chain transit mandatory. Deviation log maintained. Origin map entry revised Q3 2024 following supplier facility upgrade.
Methylcobalamin (B12)
Sourced from a globally operating documented supplier with full chain-of-custody records. Cold-chain compliant. Verification cycle: every production run.
Cholecalciferol (D3)
Oil-based D3 from a lanolin source. Supplier documentation confirmed. Each delivery accompanied by purity assay. Annual supplier re-qualification mandatory.
Selenomethionine
Regional source preferred. Cold-chain required. Elemental selenium concentration verified per batch. Revision 05-B transit log requirement applies.
Ubiquinone (CoQ10)
CoQ10 sourced from a fully documented global supplier. Purity specification: minimum 98% ubiquinone content as per the lot certificate. Independent verification confirms content per batch.
Quality & Compliance Statement
Oranevel 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.
The quality framework at Oranevel is not a marketing claim — it is an operational procedure. The six-stage process described in section 02 produces a documented record for every batch. The record is the quality system. The documentation is the evidence.
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.
Audit Schedule & Verification Frequency
Full ingredient tables, lot references, and elemental composition data across all six active formulations.