Compare CDMOs with comprehensive analytical services for release testing, stability, method development, and characterization. Filter by testing type, accreditation, and capacity.
17 companies listed
If the data isn't GMP, it doesn't count toward release or a filing — that's the whole game with analytical services. Every batch you release and every submission you make rests on analytical data: identity, assay, impurities, dissolution, sterility. A contract lab produces the evidence that your product meets spec. Cheap, non-GMP numbers can't be used for either purpose, so verify the quality system first. What are you actually buying? Release and stability testing under ICH conditions, method development and validation per ICH Q2, and the scientific depth to run down an out-of-specification result instead of just reporting it. Data integrity is now a top FDA inspection finding, so ask how they handle audit trails and chromatographic review. For biologics, confirm characterization and comparability capability, not just small molecule HPLC. 17 CDMOs here list analytical services. Compare them by testing scope, accreditation, and molecule type.
Analytical services underpin every stage of pharmaceutical development and manufacturing. From raw material testing through in-process controls to finished product release, analytical data provides the evidence that a drug product meets its specifications. GMP analytical laboratories must operate under validated methods, calibrated equipment, and documented procedures.
CDMOs offering analytical services range from full-service integrated organizations (manufacturing + analytics) to specialized contract testing laboratories. The most valuable analytical partners offer: method development and validation, release and stability testing, regulatory filing support (CTD Module 3), and the scientific depth to troubleshoot out-of-specification results.
United Kingdom
We collaborate closely with clients to design and deliver tailored in vitro studies and BITE human trials that align with specific product goals, formulation challenges, and development timelines. Whether you're working with digestive enzyme modulation, recombinant proteins or complex delivery systems, we can support you with custom-designed projects.
Czech Republic
We provide our clients, both local and international pharmaceutical and chemical companies, with services performed in a professional and timely fashion, which enables them to accomplish their research goals in drug discovery and crop protection.
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India
At Cliantha Research , we support the clinical development of biologics and biosimilars with end-to-end solutions across early- and late-phase trials. Our multidisciplinary teams combine therapeutic expertise, operational excellence, and advanced infrastructure to deliver high-quality, regulatory-compliant studies. We have strong capabilities in managing complex biosimilar study designs, including PK/PD studies, immunogenicity assessments, comparative efficacy trials, and safety evaluations. Our integrated clinical, bioanalytical, and data management services ensure seamless execution aligned with global regulatory standards.