EUTECNIQ Sciences

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Proposed lab journey Proposed layout Illustrative · nothing has been built

One traceable development pathway—from source to scientifically qualified material.

Eleven proposed stations in work order, with custody recorded at every hand-off and partner work sent and returned sealed.

72,000 sq ftproposed floor area at full build
18,000 sq ftproposed Phase I laboratory core, earliest 2027
3 phasesPhases II and III only after their gates are met
11 + partnersstations in this journey, plus off-site partner work

Status. Nothing here exists yet: no site, equipment or partner agreement. The drawings explain a proposed arrangement, not a real building.

How to read the proposed journey

  1. Every station is labeled with its proposed phase or as partner work.
  2. Custody first and last: receiving, sampling and release frame every journey.
  3. Select a room in either drawing to open the page on that work.
The drawing

Rooms are arranged in the order a sample would meet them, with partner work off site

Proposed laboratory and pilot plant, isometric cutaway Proposed layout · illustrative · not to scale

The plan is wider than this screen: scroll sideways, or use the station list below.

Proposed lab journey

Select a station, or follow one sample

Each numbered room is one step in qualifying a botanical ingredient. Select a room, or use the station list below the drawing.

Samples, results and decisions remain traceable across qualified internal and external partners.

Proposed arrangement for explanation only; rooms are not to scale and the area program is not a floor plan. Phases follow the facilities roadmap: Phase I (proposed for 2027, 18,000 sq ft) is the laboratory core; Phase II adds pilot extraction, evaporation, solvent recovery, pilot drying, a second LC-MS and walk-in stability; Phase III adds commercial manufacturing, packaging and a commercial dryer. Provisional assignment: the founder has not yet assigned a phase to receiving and milling. This page places sample receiving, quarantine, sampling and retained samples with the Phase I laboratory, and bulk raw-material milling with the Phase II pilot plant, pending founder confirmation. Items not in the phase plan are marked "not yet assigned" or "external partner".
Explanation, details and sources

Why it mattersSplit across vendors without a shared record, evidence scatters and decisions come late. One record per lot, covering in-house and partner work, is meant to shorten that loop.

All stations

Eleven stations and the off-site partners, in the order a sample meets them

A plan view of the same rooms shows where the sample changes hands; the board shows which phase would bring each piece of equipment.

The sample would change hands at every door, and each hand-off would be recordedConceptual plan · not to scale
Conceptual plan of the proposed laboratory and pilot plant: eleven rooms on one corridor in the order a sample meets them, the step numbers where the sample enters each room, a custody record at every hand-off, and off-site partner work1. Receiving, quarantine and sampling: open the page that explains this work1Receiving, quarantineand sampling4. Extraction bay: open the page that explains this work4Extraction bay5. Separation and concentration: open the page that explains this work5Separation andconcentration6. Formulation and nanoemulsion: open the page that explains this work6Formulation andnanoemulsion7. Drying: open the page that explains this work7Drying2. Identity lab: open the page that explains this work2Identity lab3. Analytical lab: open the page that explains this work3Analytical lab8. Stability chambers: open the page that explains this work8Stabilitychambers9. Microbiology: open the page that explains this work9Microbiology10. Quality release and data: open the page that explains this work10Quality releaseand data11. Pilot packaging: open the page that explains this work11Pilot packagingRecovered solventreturns to extractionSeparated suiteRetained andreserve samples1–38910104511117 · 1212PQualifiedpartners, off siteDNA barcoding,NMR, toxicology,human studies,bioanalysis, contractmanufacturing.Samples travelsealed6Receiving dockPhase IPhase IIPhase IIIPartner4Step number at the door: the sample changes hands and custody is recordedCorridor: the sample pathMirrored from the isometric drawing above so the sample enters at the left. Rooms are not to scale; bulk milling would sit in room 1 in Phase II (provisional).
Step numbers follow the twelve steps below. Proposed area program (full build): analytical chemistry and QC 7,000 sq ft; discovery and extraction labs 5,000; pilot plant 10,000; formulation R&D 5,000; microbiology, stability and QA 6,000; packaging 7,000 (Phase III).
Most laboratory equipment would arrive in Phase I; pilot equipment waits for Phase IIProposed phasing
Equipment named for each of the eleven stations and the off-site partners, sorted by the proposed phase that would bring it, a qualified partner, or not yet assignedPhase I · proposed 2027Phase II · after Gate 1Phase III · afterGate 2External partnerNot yet assigned1Receiving,quarantine andsamplingReceiving bench (prov.)Quarantine racks with status labels(prov.)Sampling booth with dust extraction(prov.)Hammer mill and sieves (prov.)2Identity labMicroscopesHPTLC fingerprintingReference specimen cabinetDNA barcoding3Analytical labHPLC and UHPLC stacksSample preparationLC-MS/MSHigh-resolution LC-MSGC-MSICP-MSSecond LC-MSNMR4Extraction bayLab supercritical CO₂ and CO₂ supplyRotary evaporatorBalancesPilot percolation vesselsUltrasound-assistedextraction bench5Separation andconcentrationFalling-film evaporator withcondenserSolvent receiver for recoveryAdsorption-resincolumnsMembranefiltration skid6FormulationandnanoemulsionHigh-pressure homogenizerDLS and laser diffractionJacketed mixing vessels7DryingLab spray dryerLab freeze-dryerPilot spray dryer, cyclone, bag filterPilot freeze-dryerFluid-bed dryerCommercial dryer8StabilitychambersReach-in chambersContinuous temperature and humidityloggingWalk-in chamber9MicrobiologyBiological safety cabinetIncubatorsAutoclavePlate-counting benchUSP <2021>–<2023>10Quality releaseand dataRecord-review stationsLIMS, electronic notebooksRetained and reserve samples11Pilot packagingBin blender (II–III)Capsule filler (II–III)Packaging conveyor (II–III)Packaging area,7,000 sq ftPOff-sitepartnersAccredited testinglabsToxicology CROsClinical researchorganizationsBioanalytical labsContractmanufacturers
"prov." marks the founder's provisional assignment of receiving and milling. Items not in the phase plan are "not yet assigned" or "external partner". Laboratory-scale concentration uses the extraction bay's rotary evaporator.
Room 8 would hold the ICH Q1A(R2) storage conditions, each within ±2 °C and ±5% RHICH guideline
ICH Q1A(R2) storage conditions as temperature and relative-humidity windows: long term 25 °C/60% RH, long term alternative or intermediate 30 °C/65% RH, accelerated 40 °C/75% RH, each held within ±2 °C and ±5% RH; refrigerated long term 5 °C ± 3 °C with no humidity condition.051015202530354045Temperature, °C30405060708090Relative humidity, %Refrigerated long term: 5 °C ± 3 °C, 12 months; no humidity condition5 ± 3 °Cany RHLong term: 25 °C ± 2 °C, 60% RH ± 5% RH; 12 monthsLong term (alternative) or intermediate: 30 °C ± 2 °C, 65% RH ± 5% RH; 12 or 6 monthsAccelerated: 40 °C ± 2 °C, 75% RH ± 5% RH; 6 monthsCondition (minimum duration atsubmission)Long term25 °C / 60% RH · 12 monthsLong term (alternative) orintermediate30 °C / 65% RH · 12 or 6 monthsAccelerated40 °C / 75% RH · 6 monthsRefrigerated long term5 °C · 12 monthsBoxes: ±2 °C and ±5% RH control windows
Source: ICH Q1A(R2), Stability testing of new drug substances and products, Step 4, February 6, 2003 (general case and refrigerated storage). A drug guideline used here as a reference for supplements; stability testing alone does not establish a validated shelf life.
Station list: what each station does, its equipment, its result and the rules that apply (with "Show on drawing")
  1. Receiving, quarantine and sampling

    Phase I · provisional Bulk milling · Phase II · provisional

    Each incoming lot is checked against its paperwork, given a unique ID, held in quarantine and sampled to an approved sampling plan. Part of each sample is retained.

    Equipment
    • Receiving bench and quarantine racks with status labels Phase I · prov.
    • Sampling booth with dust extraction Phase I · prov.
    • Hammer mill and sieves for bulk milling Phase II · prov.
    Result
    A logged, quarantined lot with representative samples, and a custody record that every later result points back to.
    Rules
    21 CFR 111.155 (receipt, quarantine); 21 CFR 111.80 (representative samples).

    Particle size and extraction time (science lab)

  2. Identity lab

    Phase I DNA barcoding · partner

    Confirms the plant is the right species and plant part before any other work starts.

    Equipment
    • Microscopes Phase I
    • HPTLC fingerprinting and documentation Phase I
    • Reference specimen cabinet Phase I
    • DNA barcoding External partner
    Result
    An identity decision for every lot. The rule requires at least one identity test of each dietary-ingredient lot (21 CFR 111.75(a)(1)(i)); the plan uses two independent methods.

    How identity methods work (discovery and characterization)

  3. Analytical lab

    Phase I Second LC-MS · Phase II NMR · partner

    Measures what is in the material: marker compounds, adulterants, metals, pesticides and residual solvents.

    Equipment
    • HPLC and UHPLC stacks, sample preparation Phase I
    • LC-MS/MS and high-resolution LC-MS Phase I
    • GC-MS; ICP-MS for elemental impurities Phase I
    • Second LC-MS Phase II
    • NMR External partner
    Result
    Composition and contaminant results, compared with specifications.
    Floor area
    Analytical chemistry and QC, 7,000 sq ft in the proposed full-build area program.

    Instrument principles (analytical characterization)

  4. Extraction bay

    Lab scale · Phase I Pilot · Phase II

    Pulls the active compounds out of the plant with ethanol–water or supercritical CO₂.

    Equipment
    • Laboratory supercritical CO₂ extraction and CO₂ supply Phase I
    • Rotary evaporator and balances Phase I
    • Pilot percolation vessels Phase II
    • Ultrasound-assisted extraction bench Not yet assigned
    Result
    A crude extract with measured yield and composition, reported separately: a high yield is not a high purity.
    Floor area
    Discovery and extraction labs, 5,000 sq ft; pilot plant, 10,000 sq ft (proposed area program).

    Extraction methods and curves (extraction and purification)

  5. Separation and concentration

    Lab scale · Phase I Pilot equipment · Phase II

    Removes the solvent for reuse, then concentrates or purifies the extract. Laboratory-scale concentration uses the extraction bay's rotary evaporator.

    Equipment
    • Falling-film evaporator with condenser Phase II
    • Solvent receiver for recovery Phase II
    • Adsorption-resin columns Not yet assigned
    • Membrane filtration skid Not yet assigned
    Result
    A concentrated extract, and recovered solvent returned to extraction.

    Mass and energy balances (process engineering)

  6. Formulation and nanoemulsion

    Phase I Pilot vessels · Phase II

    Turns the extract into a stable, dosable form: emulsions, dispersions and encapsulates.

    Equipment
    • High-pressure homogenizer Phase I
    • Droplet sizing by dynamic light scattering and laser diffraction Phase I
    • Jacketed mixing vessels Pilot scale · Phase II
    Result
    Formulations with measured droplet size and physical stability. Neither is evidence of absorption in people.
    Floor area
    Formulation R&D, 5,000 sq ft (proposed area program).

    Emulsion science (emulsions and colloids)

  7. Drying

    Lab · Phase I Pilot · Phase II Commercial · Phase III

    Turns a liquid into a stable powder without overheating the actives.

    Equipment
    • Laboratory spray dryer and freeze-dryer Phase I
    • Pilot spray dryer with cyclone and bag filter; pilot freeze-dryer; fluid-bed dryer Phase II
    • Commercial-scale dryer (not drawn) Phase III
    Result
    Free-flowing powder with measured moisture, ready for blending.

    Spray and freeze drying (drying and particle engineering)

  8. Stability chambers

    Phase I Walk-in chamber · Phase II

    Stores samples at set temperature and humidity to see how long they stay within specification.

    Equipment
    • Reach-in chambers with continuous temperature and humidity logging Phase I
    • Walk-in stability chamber Phase II
    Result
    Stability data, the evidence needed before a shelf life can be set. Accelerated data alone do not validate a shelf life.
    Floor area
    Shares microbiology, stability and QA, 6,000 sq ft (proposed area program).

    Accelerated stability calculator (science lab)

  9. Microbiology

    Phase I

    Tests materials and products for microorganisms and compares results with microbial limits, in a separated suite.

    Equipment
    • Biological safety cabinet, incubators, autoclave, plate-counting bench Phase I
    • Compendial methods, USP <2021>–<2023> Phase I
    Result
    Microbial results for every lot before release.

    Contamination control (quality system)

  10. Quality release and data

    Phase I

    Quality control reviews every record and releases or rejects each lot. All results, including partner results, land in one data system. Retained and reserve samples are stored here.

    Equipment
    • Record-review stations; LIMS and electronic notebooks Phase I
    • Retained and reserve sample storage Phase I
    Result
    A release decision and one complete record per lot. Quality control makes disposition decisions (21 CFR 111.87); reserve samples of packaged supplements are kept as 21 CFR 111.83 requires.

    Specification and release workflow (quality system)

  11. Pilot packaging

    Phase II Phase III

    Blends released material and fills it into capsules or powders, then packs it.

    Equipment
    • Bin blender, capsule filler, packaging conveyor Phase II–III
    Result
    Packed, labeled product from released lots only.
    Floor area
    Packaging, 7,000 sq ft (proposed area program, Phase III).

    Scale-up and technology transfer (process engineering)

  12. Qualified external partners, off site

    External partner

    Work outside the planned in-house scope would go to qualified partners: DNA barcoding, NMR, toxicology studies, human studies, plasma bioanalysis and, until Phase III, commercial-scale manufacturing.

    Partners
    • Accredited testing laboratories (scope checked per test) Partner
    • Toxicology CROs, GLP where appropriate Partner
    • Clinical research organizations and bioanalytical laboratories Partner
    • Contract manufacturers Partner
    Result
    Partner results return to the same lot record and are reviewed by EUTECNIQ quality before use. No partner agreement is signed.

    Partner-led safety studies (toxicology and exposure)

Follow one sample

Twelve steps from the receiving dock to a released lot, with custody kept at every hand-off

The rules cited are legal minimums for dietary-supplement manufacturing; the rest is proposed practice. "Follow one sample" walks the drawing through the same steps.

Twelve steps across five areas, with three quality-control decisionsProposed workflow
Twelve steps from the receiving dock to a released lot, laid out across seven lanes; each change of lane is a custody hand-off that would be recordedReceiving andquarantineStation 1LaboratoriesStations 2, 3, 8, 9Off-site partnersPQuality controlStation 10Process and packagingStations 4–7, 11Rule, 21 CFRReceive and logSeals and paperworkchecked; unique lot ID1111.155(a)–(b)QuarantineHeld, physically and inthe records2111.155(c)Sample and retainApproved plan; oneportion retained3111.80, 111.315Confirm identityA wrong plant stopshere4Measure compositionMarkers, adulterants,metals, pesticides,solvents5Specialist tests outSealed, with custodyform; results return6Approve or reject thelotOnly then does it leavequarantine7111.155(c)Mill and extractMilling at pilot scale(Phase II, prov.)8Concentrate andpurifySolvent recovered forreuse9Formulate and dryMeasured droplet size;stable powder10Stability andmicrobial qualityChambers;microbiology againstlimits11Release or reject;retainComplete recordreviewed; reservesamples kept12111.87, 111.83Pack releasedmaterialOnly released materialis packedStopHand-off between areas: custody recorded (who released, who received, date, time, location)Quality-control decision
eCFR, 21 CFR 111.80, 111.83, 111.87, 111.155, current to Oct 21, 2026.
Text version of the twelve steps
  1. Receive and logContainers are checked for damage and broken seals, paperwork is checked against the purchase order, and the lot gets a unique ID that every later record uses (21 CFR 111.155(a)–(b)).
  2. QuarantineThe lot is held under quarantine status, physically and in the records, until quality control approves it for use (21 CFR 111.155(c)).
  3. Sample and retainRepresentative samples are drawn to a sampling plan approved by quality control (21 CFR 111.80(a), 111.315(b)). One portion goes to testing; another is sealed, labeled and retained for investigations.
  4. Confirm identityMicroscopy and HPTLC confirm species and plant part against authenticated references. A wrong plant stops here.
  5. Measure compositionChromatography and mass spectrometry measure markers, adulterants, metals, pesticides and residual solvents.
  6. Send specialist tests outTests outside the planned scope, such as DNA barcoding or NMR, go to qualified partners. Samples travel sealed with a chain-of-custody form; results return to the same lot record.
  7. Approve or reject the lotQuality control reviews all results and approves the lot for use or rejects it (21 CFR 111.155(c)). Only then does it leave quarantine.
  8. Mill and extractAt pilot scale, approved material is milled to a set particle size (Phase II, provisional), then extracted with ethanol–water or supercritical CO₂.
  9. Concentrate and purifyThe solvent is evaporated and recovered for reuse; resins or membranes may clean up the extract.
  10. Formulate and dryThe extract becomes an emulsion or dispersion with a measured droplet size, then a stable powder.
  11. Prove stability and microbial qualitySamples go into stability chambers and through microbiology testing against limits.
  12. Release, retain and packQuality control reviews the complete record and releases or rejects the lot (21 CFR 111.87). Reserve samples are kept as the rule requires (21 CFR 111.83). Only released material is packed.
Chain of custody

Custody would be recorded at every hand-off, inside the building and across partner sites

Five fields for every sample, and a sealed round trip for partner workProposed practice
The custody record for every sample has five parts; a sample sent to a partner travels sealed with a signed form and comes back as results that quality reviews before useCustody record, every sampleIdentityUnique ID linked to the parent lot, supplierand purchase orderEvery transferWho released it, who received it, date, timeand locationConditionCondition on receipt, seal numbers andstorage conditionsTestingTests requested, the laboratory and themethod versionRetentionRetention location, retention period and finaldisposal1Seal and signTamper-evident container;signed custody form;temperature record whereneeded2Partner confirmsreceiptCondition checked;accreditation scope orstudy status checked forthat test3Results into the lot recordThe same record that holdsin-house results4Quality reviewBefore any decision uses theresultsSample outResults returnEUTECNIQQualified partner, off siteProposed practice. No partner agreement is signed.
Proposed practice built on 21 CFR 111.155, 111.80 and 111.83 and ISO/IEC 17025:2017 clause 7.4 (as summarized by ANAB); no partner agreement is signed.
How a tamper-evident custody record works: edit any field and the chain no longer verifiesSimulation · example values
A hash chain is one data-integrity technique; no regulation requires it. 21 CFR Part 11 and ALCOA+ require records that are attributable, complete and auditable. Example values only; EUTECNIQ holds no records. More on the digital lab page.
Text version of the custody record and the partner hand-off

What would be recorded for every sample

  • A unique ID linked to the parent lot, supplier and purchase order.
  • Each transfer: who released it, who received it, date, time and location.
  • Condition on receipt, seal numbers and storage conditions.
  • Tests requested, the laboratory and the method version used.
  • Retention location, retention period and final disposal.
Proposed practice

When a sample goes to a partner

  • A signed chain-of-custody form travels with the sample in a sealed, tamper-evident container.
  • A temperature record travels with materials that need it.
  • The partner confirms receipt and condition; its scope of accreditation or study status is checked for that test.
  • Results return to the lot record and are reviewed by EUTECNIQ quality before any decision uses them.
Proposed practice

Sources: eCFR, 21 CFR 111.80, 111.83, 111.155, 111.465, 111.605, current to Oct 21, 2026; ANAB, "ISO/IEC 17025:2017 process requirements" (summary of clause 7.4). Retained samples of incoming components are proposed practice, not a Part 111 requirement.

Explanation, details and sources

Chain of custody is the unbroken record of who held a sample, when, where and in what condition. It lets a result be trusted when the work is split between EUTECNIQ and its partners.

Requirement or standardWhat it requiresApplies to
21 CFR 111.155 Regulatory requirementExamine containers and paperwork on receipt; quarantine components until representative samples are collected and quality control approves them.Components of dietary supplements
21 CFR 111.80 Regulatory requirementCollect representative samples of each unique lot of components, packaging and labels, and of each unique shipment.Dietary-supplement manufacturing
21 CFR 111.83 and 111.465 Regulatory requirementHold reserve samples of each lot of packaged and labeled supplement in the distributed container-closure system, for 1 year past the shelf-life date or 2 years from distribution of the last batch.Packaged and labeled dietary supplements
21 CFR 111.605 Regulatory requirementKeep required records for the same period; electronic records must meet 21 CFR Part 11.Records required by Part 111
ISO/IEC 17025:2017, clause 7.4 Planned accreditationA procedure for transport, receipt, handling, protection, storage, retention and disposal or return of test items, with a system for identifying them.An accredited laboratory's scope; EUTECNIQ holds no accreditation

See how the gates decide what moves on

The platform page sets out each stage's objective, gate and failure modes; the quality system page sets out the rules that would govern release.