Custom method and matrix review

Define an analytical plan for unusual matrices, new targets, combined questions, or projects that do not fit a standard starting pathway.

Suitable for

Supplements, cosmetic actives, raw materials, intermediates, finished products, complex formulations, unusual compounds, and multi-part analytical questions.

Typical output

Written testing recommendation, feasibility findings, sample requirements, quotation, and—when accepted—scope-specific analytical results.

Service overview

Custom work begins with the decision the result needs to support. Odyssey Standards reviews the target, matrix, expected range, available references, sample amount, timeline, and reporting needs before recommending a pathway.

The first phase may be a document review, feasibility screen, method selection exercise, limited trial, partner-laboratory inquiry, or a staged project. No experimental work begins until the applicable scope is accepted.

Questions this service can address

The exact question is recorded before testing so the method and report remain tied to the intended scope.

What analytical result would meaningfully answer the project or quality question?
Is there an existing method or reference strategy that can be applied or adapted to the matrix?
Should the work be divided into feasibility, method evaluation, and sample-analysis phases?
Which parts of the project can be performed directly and which may require a disclosed specialist partner?

What shapes the scope

These details affect feasibility, method selection, sample requirements, interpretation, and pricing.

Target analytes, expected ranges, likely interferences, and required reporting units
Complete formulation or matrix information and any known handling hazards
Available standards, methods, literature, specifications, or prior analytical data
Sample amount, number of lots or units, homogeneity, storage, and shipping conditions
Decision criteria, timing, budget, data package, and revision expectations

What to provide

More complete project information produces a more useful scope and reduces avoidable delays.

Plain-language description of the question and the decision it will support
Target compounds, expected levels, and all available matrix or formulation details
Lot or batch information and available sample quantity
Relevant methods, standards, specifications, literature, or prior results
Timeline, report format, and any required third-party or regulatory method constraints

Typical deliverables

The accepted scope identifies the exact report, COA, chromatogram, calculation note, partner documentation, or other data package to be issued.

Written feasibility or testing-pathway recommendation
Defined phases, sample requirements, timing estimate, and quotation
Disclosure of proposed partner-laboratory work when applicable
Scope-specific analytical report or COA for accepted testing phases
Observations, revision status, supporting data, and limitations appropriate to the project

Important limitations

Results should be read with the method, sample description, report notes, and revision status.

A feasibility review may conclude that the requested measurement is not supportable with the available sample, references, method, timing, or laboratory capability.

Exploratory or development work may not produce a routine-ready method or definitive result; phase objectives and decision points are therefore defined in advance.

Custom analytical findings apply to the submitted material and accepted scope and should not be extended to other samples, lots, products, or uses without supporting work.

Ready to discuss this testing pathway?

Send the sample details and analytical question first. Do not ship until the project is accepted.

Request scope review