From your first raw materials to your release-ready batches, we rigorously evaluate and verify your product’s quality at key steps throughout the manufacturing process. Explore the robust testing methodologies we offer.
The quality of your finished product depends on the quality of starting your materials – which is why we sample and test every excipient, ingredient, and packaging component to ensure it meets regulatory requirements and customer specifications.
We use a wide range of testing to verify the identity, authenticity, purity, and conformance of incoming goods we receive at our facilities. Find out how we maintain the strictest possible quality control.
Before finished products leave our facilities, they pass through rigorous, cGMP-compliant controls designed to ensure every unit meets the highest possible quality standards.
From microbiology, to bioanalytics, and physico-chemical methods, our product testing are always fully aligned with your validated specifications, EMA requirements, and FDA regulations. See how we customize them to your unique product.
Stability data play an essential role in your product’s success, from regulatory submissions, to global distribution, to long-term integrity in storage. We gather and evaluate that data regularly, checking that we’re aware of any risks and prepared to safeguard both your product and the patients who use it.
Take a closer look at how we tailor stability programs and storage conditions to your product’s specific needs.
Vetter’s Analytical Testing Services cover comprehensive analytical testing across the entire drug product lifecycle – from raw materials to release-ready batches.
Our analytical testing verifies quality at every step of the manufacturing process. These services support API, raw material, and packaging quality, verify product and process performance, evaluate stability and sterility, and support batch release.
Vetter controls drug product quality using cGMP‑compliant analytical methods.
Finished drug product units are tested with validated methods aligned with EMA, FDA, ICH, and USP requirements.
We provide both compendial and customized product‑specific analytical testing methods across microbiology, bioanalytical testing, and physico‑chemical testing. This tailored method spectrum supports regulatory compliance throughout incoming control, in‑process control, and final batch release.
Vetter offers a wide range of analytical testing services, including:
Vetter verifies the quality of incoming materials by sampling and testing excipients, API drug substances, as well as primary and secondary packaging components.
Identity, authenticity, purity, and regulatory compliance are tested using a wide range of analytical methods. This supports consistent quality control from incoming materials through final batch release.
Vetter supports stability studies with state-of-the-art, qualified climate chambers and customer-tailored testing regimes.
Stability data are generated from real‑time, accelerated, and intermediate studies in accordance with ICH guidelines. These data ensure patient safety and define appropriate storage conditions and shelf life.
For development, process control, and batch release, Vetter provides microbiological sterility data as well as physico‑chemical and bioanalytical analysis.
We also test the long‑term integrity of packaging combinations in commercial drug products under various storage conditions.
