Raw-material identity, in-process QC, endotoxin and mycoplasma screening, elemental impurities, and finished-product release testing — with documentation your auditors will accept.
From incoming raw materials to final release, IAS gives pharmaceutical and biotech manufacturers the analytical depth — and the turnaround — to keep production on schedule and inspectors satisfied.
Whether you are qualifying a new excipient supplier, investigating an out-of-spec result, or running routine release testing, our chemists work alongside your QC team rather than behind a portal.
Standard analyses carry catalog pricing, repeat submissions are simple once an account is open, and one-off investigations are always welcome.
We run to recognized compendial and ICH expectations, with reporting and chain-of-custody suited to audited environments.
A representative slice of routine pharma work — anything compendial or custom can be quoted on a call.
| Test / Analysis | Typical method | From |
|---|---|---|
| Elemental impurities panel (ICH Q3D) | ICP-MS | Call to quote |
| Bacterial endotoxin (LAL) | Kinetic / gel-clot | $140 |
| Mycoplasma screening | Culture / PCR | Call to quote |
| Residual solvents | GC-MS | $175 |
| Compound / API identity | NMR | $325 |
| USP purified water suite | Conductivity · TOC · microbial | $165 |
Detects and quantifies trace and ultra-trace metals down to parts-per-trillion levels.
Determines molecular structure and confirms compound identity.
Identifies organic & inorganic compounds through molecular fingerprinting.
No formal account is required to send your first sample for evaluation.
Call or email with a description of what you're testing and what you're looking for. Not sure which test? We'll help you figure it out.
We tell you exactly what to collect, how to collect it, and how to ship it — and we'll supply the bottles and collection materials if you need them.
Your sample is logged, analyzed by our experienced team, and results are delivered clearly — with context whenever you need it.
Submit a one-time sample with zero setup. Need ongoing testing? We'll open an account that makes repeat submissions simple.
Our chemists and chemical engineers will walk through your situation and help you design the right approach — at no charge.
Yes. We run ICH Q3D elemental impurity panels by ICP-MS on drug substances, excipients, finished products and process water, with reporting against your established permitted daily exposures.
Absolutely. Many pharmaceutical clients run scheduled release and stability-support testing with us. We open a simple account so repeat submissions and reporting stay consistent.
Yes — kinetic and gel-clot LAL endotoxin testing and mycoplasma screening to support biologics, sterile products and medical-device clients.
We do. Custom method development and validation support is part of our routine work, including non-compendial impurities and difficult matrices.
No. You can submit a one-time sample for investigation or qualification without opening an account.
Method transfer, a non-compendial impurity, a stubborn excipient matrix, or a deviation investigation — we develop and run custom analytical methods for pharma and biotech, and you can send a single sample without ever opening an account.
Talk to a chemist about your release, raw-material or impurity testing — most consultations are included at no charge.