About Motark

Operations & Compliance

Corporate, regulatory, and counterparty reference.

Hong Kong corporate registration, operating model, quality and regulatory framework coverage, counterparty diligence procedure, documentation policy, and insurance cover.

01 · Corporate

Corporate registration.

The entity counterparties contract with. Beneficial-ownership disclosure and corporate-identity documentation available to verified reviewers on request, under NDA.

Registered name
Motark Enterprise Limited (摩達企業有限公司)
Hong Kong CR
2338553
Business registration
65775040
Incorporated
4 February 2016
Registered office
Unit J, 9/F., King Palace Plaza, 55 King Yip Street, Kwun Tong, Kowloon, Hong Kong
Banking jurisdiction
Hong Kong (HKMA-regulated tier)
Murray-Brown Laboratories — per-batch analytical work.
Lab partner
Murray-Brown Laboratories — Northglenn, CO
Scope
ISO 17025 · heavy metals · microbial · pesticide residues

02 · Operating model

Operating model.

Motark operates an asset-light, partner-network model. We do not own primary processing or analytical facilities directly. Capabilities are accessed through long-term contractual relationships with vetted partner laboratories, contract manufacturers, and cooperatives direct with growers across six sourcing regions.

01

Capital efficiency without quality compromise

Partner facilities operate at scale we could not match independently. Each is selected for its specific specialisation — pre-processing in Thailand and Fiji, extraction in India, ISO 17025 analytical work in EU and US labs, and fermentation in Southern Africa.

02

Multi-jurisdictional regulatory coverage

Operating through partner organisations in multiple jurisdictions gives our counterparties a structural advantage: documentation packages can be assembled to FDA, EFSA, TGA, HKMA, or ASEAN standards from the partner with the relevant local approval, rather than re-engineering from a single base.

03

Speed to specification

Custom extraction briefs that would require capacity expansion at an integrated manufacturer typically reach feasibility within two weeks through our partner network. Pilot batches in 6–10 weeks; commercial supply in 12–20 depending on jurisdiction.

03 · Quality systems

Certifications and standards.

Quality posture is operated through partner facilities — each carries the relevant certification per its specific scope of work. Motark coordinates the certification matrix at the counterparty level. Underlying audit reports are available to verified reviewers.

GMP

GMP-aligned operations

Issuer
Per partner facility — WHO-aligned and ICH Q7
Scope
All partner extraction, processing, and packaging operations
ISO 9001

Quality Management Systems

Issuer
Accredited certification bodies (per partner)
Scope
Quality management at processing partners
HACCP

Hazard Analysis and Critical Control Points

Issuer
Per partner facility
Scope
Food-grade extract operations
ISO 17025

Analytical laboratory competence

Issuer
Accredited third-party laboratories (EU and US)
Scope
Per-batch analytical verification — heavy metals, pesticide residues, microbial, assay
ISO 22000

Food Safety Management

Issuer
Per partner facility (where food-grade)
Scope
Food-grade extract operations
GACP

Good Agricultural and Collection Practices

Issuer
WHO-aligned, verified at intake
Scope
Origin sourcing operations

Named analytical partners

Per-batch testing laboratories.

Independent, accredited third-party laboratories engaged for per-batch analytical work. Underlying accreditation certificates and current scope documents available to verified reviewers on request.

Laboratory

Murray-Brown Laboratories

Northglenn, Colorado, USA

Accreditation

ISO/IEC 17025:2017 — annually audited. CDPHE certifications: Hemp Metals, Hemp Microbials, Drinking Water Microbiology. Third-party proficiency-testing programmes: AOAC, LGC, NSI, Phenova, NIST.

Motark scope

Heavy metals, pesticide residues, microbial profiling, and regulatory dossier support.

Laboratory

Wonderland Labs

Vista, California, USA

Accreditation

A2LA-accredited ISO/IEC 17025 — chemical analysis and microbiological analysis on food products.

Motark scope

Identity verification, contaminants, and pathogen screening.

Laboratory

Cora Science

Austin, Texas, USA

Accreditation

ISO/IEC 17025:2017 — accredited by Perry Johnson Laboratory Accreditation (PJLA). Current status verifiable on the PJLA accredited-organisation register.

Motark scope

Botanical-specific HPLC/UHPLC and GC-MS — kavalactones, bacosides, mesembrine-type alkaloids, and related botanical actives.

Accreditation status is verifiable directly with each issuing body. Additional partner laboratories engaged on a per-jurisdiction basis are disclosed to verified counterparties on request.

04 · Regulatory

Markets in active supply.

Motark supplies into these jurisdictions through its partner network. Documentation packages are structured to each importer's local requirements and made available to verified counterparties on request.

Market

United States

Framework

FDA — Dietary Supplement Health & Education Act

Motark posture

NDI notification framework where applicable. Documentation packages structured for 21 CFR §111 compliance.

Market

European Union

Framework

EFSA — Regulation (EU) 2015/2283 (Novel Food)

Motark posture

Compounds with novel-food status reviewed per partner-specific submissions; counterparty advised pre-supply.

Market

Australia

Framework

TGA — Therapeutic Goods Administration

Motark posture

Listed-medicine ingredient framework; AUST L documentation packages available on request.

Market

Hong Kong

Framework

HKMA · Centre for Food Safety

Motark posture

Banking and counterparty workflow aligned to HKMA expectations. Food-grade extract framework via CFS.

Market

ASEAN

Framework

Harmonised ASEAN traditional medicine framework

Motark posture

Per-jurisdiction documentation; regional supply contracts adapted to importer's local requirements.

05 · AML / KYC posture

Counterparty diligence procedure.

Some compounds in Motark's register carry jurisdictional sensitivity. The intake workflow below documents how we vet counterparties before any engagement and how that hygiene supports our banking relationships.

01

Counterparty verification — all engagements

Business email verification, registered organisation lookup, and intended-use declaration before any engagement. This is the baseline for sample shipments and document releases.

02

Bank-led KYC and sanctions screening — commercial engagements

The foundation of a commercial supply contract or licensing arrangement. Counterparty information — including beneficial-ownership disclosure — is collected and provided to our banking partner to support inbound payment clearance and the bank's formal KYC. Sanctions and PEP screening (OFAC, UK HMT, EU consolidated, HKMA) sits with the bank as standard banking practice.

03

Source-of-funds documentation — high-value commercial

For supply contracts above HKD 1m or for licensing arrangements: source-of-funds documentation requested from the counterparty per banking-partner guidance and provided to the bank for compliance review.

04

Banking partner alignment

Counterparty workflow designed in consultation with our banking partners. Material changes to risk classification or jurisdictional exposure trigger pre-engagement review.

06 · Documentation

Documentation policy.

Uniform across compounds and counterparties. Records retained on Motark systems as per regulatory guidance.

Certificate of Analysis (COA)
Issued per batch, retained 7 years
Heavy metals report
Per batch — Pb, As, Cd, Hg
Pesticide residue report
Per batch — USP <565> / EU MRL panels
Microbial testing report
Per batch — TPC, Y&M, E. coli, Salmonella
Stability data
On request, per compound and packaging
Country of origin certificate
Per consignment, partner-issued
Material Safety Data Sheet (MSDS)
Per compound, current revision
Regulatory dossier
Available on request — verified counterparties only
AML/KYC counterparty documentation
Compiled on request — banking and institutional reviewers

For institutional reviewers

Diligence documents on request.

Tell us what you need — registration, certifications, AML/KYC workflow detail, insurance certificates, or historical audit summaries — and we'll supply the relevant documents to verified reviewers.