Counterparty Risk

Identify the company and the production site.

Compare the contracting business with the relevant public records and the site proposed for observation.

Connect the company to the records

Agree which licences, registrations or other records are relevant before the work begins. The agreed check starts after written quotation, payment and authorisation.

Where an intermediary is involved, identify the producer and document the relationship.

Establish what can be observed

If the agreed production activity cannot be observed, that is the finding. It is delivered in writing.

TEKMERIS does not source, select or recommend suppliers, or take factory commissions.

For clinics

Hospitals, clinics and wellness operators

Request a dated facility visit or observation of agreed production activity for consumables and devices. Each request needs its own scope, access and competence review.

TEKMERIS does not source medicines or recommend treatment.

For brands

Brands and private-label businesses

Record agreed production activity and controlled sealing of the covered packaging. Optional laboratory evidence is identified separately. Each later batch or separately scoped activity requires its own engagement, including under a repeat-service arrangement.

For acquisition teams

Acquisition and procurement teams

Compare the stated supplier relationship with the contracting entity, relevant records and proposed production site. The report states what was observed and where access or evidence was unavailable.

Optional laboratory evidence.

How optional testing works

Testing is optional and performed by an independent laboratory. If requested, the factory sends samples directly to the client’s nominated laboratory under written instructions.

TEKMERIS coordinates the agreed dispatch. TEKMERIS Global does not physically store or take custody of peptide products.

What the report covers

A report covers the identified samples and tests, not every sealed package. Linking it to a batch requires the report source, reference and supporting sample-to-batch records.

Observation and sealing can be completed without testing, subject to the agreed scope and release requirements. Where no report is recorded, the record states: No laboratory report recorded.

Illustrative laboratory with analytical instruments, a microscope and sample vials
OPTIONAL LABORATORY EVIDENCE
Engagement model

Each engagement has a defined scope, identified production activity or facility and dated report. Repeat-service arrangements cover separate engagements, not general approval of a factory or future batches. Start with an access check; any refusal and reason supplied are recorded without inferring wrongdoing.

Clients are informed of the confirmed schedule and site-access arrangements for the TEKMERIS observer. Findings and progress assessments remain private until the report is complete, reviewed and signed.

Enquire about a site visit

Responsibilities at a Glance

TEKMERIS records the agreed observations and package-sealing activity. The relevant buyer, importer, supplier and logistics provider remain responsible for the requirements that apply to their own roles. TEKMERIS does not provide customs clearance or import services.

TEKMERIS: observation & controlled sealing Relevant parties: import, permits & end use Producer: product & export duties