Compounding for
clinical research
Study medication, prepared and documented to the standard your protocol demands, from feasibility review through final visit.
Verified Pharmacy Program inspected
Inspected under the National Association of Boards of Pharmacy program, with licensure in all 50 states and DC.
Cleanrooms beyond the standard
ISO-5 performance exceeded in every hood, USP <800> hazardous-drug handling in place, LegitScript certified.
One partner for your study drug, from feasibility to final resupply
The lab and the discipline your trial needs
Sterile and non-sterile preparations
Prepared in ISO-5 hoods that exceed USP <797>, with USP <800>-compliant handling of hazardous drugs.
Ingredients from qualified suppliers
Traced lot by lot, with certificates of analysis on file.
Blinding, matched placebo and kit labeling
Aligned with your randomization scheme.
Compounders with cGMP experience
Trained for both sterile and non-sterile work.
Made to protocol
Investigational preparations rarely fit a catalog. We compound to the strength, form and batch size your study design calls for, and change with it as the protocol amends.
- A range of strengths
- Multiple dosage forms
- Various routes of administration
- Excipient and base selection
- Blinded or unblinded product
- Batches sized to enrollment
From protocol to pharmacy manual
Feasibility review
We review your protocol and confirm what we can prepare, package and document.
Preparation plan
Formulation, blinding and labeling plan, agreed with your team before anything is made.
Supply & support
Reliable resupply and responsive communication through study close-out.
The people behind your study
Jack Korbutov
Built AOM from 400 sq ft in 2012 into a 50-state licensed sterile facility.
Gina Avalone
Leads discovery and turns clinical ideas into workable formulations.
Melissa King
15 years compounding, 7 years cGMP, published researcher and medical communicator.
Colleen Huzinec
Five publications and years of translating science into patient-ready language.
Clinical trial questions, answered
Anything else, ask us in the form below and a pharmacist will reply.
Yes. We compound the active preparation and a placebo matched for appearance, taste and handling, and package both under blinded kit labels aligned with your randomization scheme.
Sterile and non-sterile forms: injectables, capsules, troches, topicals and more, at the strengths the protocol specifies. If a form or strength isn't feasible we say so at the feasibility review, not after.
We are licensed in all 50 states and DC, so a single pharmacy can supply every US site in your study.
Batch records, certificates of analysis for ingredients, beyond-use dating with its rationale, and the stability considerations your monitors will ask for.
As small as your enrollment needs. Compounding is made to order, so we can match early-phase quantities and scale as the study grows, without minimum runs.
Send the basics through the form below. We review the protocol, confirm feasibility, agree a preparation plan with your team, and only then start making anything.
Tell us about your study
Share the basics and our team will schedule a feasibility conversation.
Thanks, we'll be in touch
Our team will reach out to schedule a feasibility conversation.
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