Identity & potency
Confirm the correct active ingredient and quantify its strength in raw materials and finished products.
- HPLC / UHPLC
- LC-MS & GC-MS
- FTIR identification
- Content uniformity
Medication & supplement specialists
We test medications, dietary supplements, raw materials, and finished products for identity, strength, purity, and safety—then turn complex data into decisions your team can act on.
Identity
Potency
Purity
Example only
Final reports depend on the selected method, sample, and specification.
From early formulation through lot release, we help product teams answer the questions that matter:
Testing capabilities
Choose a single test or build a program around your formulation, quality goals, and release timeline.
Confirm the correct active ingredient and quantify its strength in raw materials and finished products.
Screen for unwanted compounds and verify that products meet defined safety specifications.
Assess microbial quality across ingredients, dosage forms, and supplement categories.
Understand how quality changes over time and how a product performs under defined conditions.
What we test
Our laboratory mainly supports medication and supplement testing, with protocols tailored to each dosage form and product stage.
Discuss your productTablets, capsules, liquids, topicals, and active pharmaceutical ingredients.
Vitamins, minerals, botanicals, probiotics, powders, gummies, and softgels.
Supplier verification, incoming quality control, and compendial testing.
Method development, formulation support, troubleshooting, and pilot batches.
Quality without ambiguity
Method selection, reporting format, sample quantity, and acceptance criteria are confirmed before work begins.
Tell us what the result needs to support: development, supplier qualification, investigation, or release.
Testing can use a suitable compendial, published, transferred, or newly developed method where appropriate.
Acceptance criteria and reporting expectations are documented before samples are processed.
The final reporting package is matched to the agreed scope and the information your team needs.
A clear path to results
A dedicated project lead keeps the work moving and makes sure you always know what comes next.
Share your product, specifications, and timeline. We confirm methods, sample needs, and pricing.
Receive simple submission instructions and ship to our controlled sample receiving team.
Your study moves through analysis, data verification, and independent quality review.
Receive a certificate of analysis and talk through findings with a scientist when needed.
Timing depends on the method, sample matrix, number of samples, and reporting needs.
About Asteria
Asteria Analytical Labs focuses on testing support for medication, supplement, raw-material, and finished-product teams.
Each inquiry starts with the product, the question, and the evidence needed. The testing scope is then defined around the sample matrix and intended use of the result.
Common questions
Still unsure what to request? Send us your product details and we’ll help define the testing plan.
It depends on the dosage form and test panel. We confirm the exact quantity in your quote so you never ship more than necessary.
Yes. Share the product, ingredients, specifications, intended market, and the decision you need to make. A scientist will recommend an appropriate scope.
Yes. We routinely test active ingredients, excipients, botanicals, premixes, bulk materials, and finished dosage forms.
Yes. Method development and validation are available when a suitable compendial or published method does not exist for your product matrix.
Yes. Final reports include sample identification, method references, specifications when provided, results, and quality approval.
Start a project
Your inquiry is sent securely to the Asteria project inbox. Include the product type, test or decision needed, sample count, and target date when known.
We review the request, identify any missing information, and reply to the work email you provide.