Capability
Analytical Services CDMOs
Compare CDMOs with comprehensive analytical services for release testing, stability, method development, and characterization. Filter by testing type, accreditation, and capacity.
873 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. 873 CDMOs here list analytical services. Compare them by testing scope, accreditation, and molecule type.
About Analytical Services
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.
Companies (873)
Selkirk Pharma
United States
Selkirk Pharma is a US-based sterile fill/finish contract manufacturing organization (CMO) located in Spokane, Washington. Purpose-built by fill/finish industry experts, Selkirk offers liquid-filled vial manufacturing (0.5mL to 50mL) with fully automated isolator filling, achieving >99% yield. The facility is harmonized for GMP regulatory compliance with US FDA and EU Annex 1 standards, with capacity for both clinical trials and commercial-scale production.
Fill/Finish (Vials)Aseptic ProcessingSterile Fill/Finish
Senn Chemicals AG
Switzerland
Senn Chemicals AG is a Swiss CDMO specializing in peptide APIs, peptide fragments, amino acid derivatives, and small molecules. Founded in 1963 in Dielsdorf near Zurich, the company provides cGMP custom manufacturing services from early research to commercial phase. Senn Chemicals has been inspected multiple times by the US FDA and was acquired by Granules India in 2025 to expand peptide therapeutics and CDMO capabilities.
Frequently Asked Questions
What analytical services do pharmaceutical CDMOs typically offer?+
Core services include: raw material identity and purity testing, in-process testing, finished product release testing (assay, impurities, dissolution, content uniformity), stability studies (ICH conditions), method development and validation (per ICH Q2), extractables and leachables studies, microbiology testing (sterility, endotoxin, bioburden), and specialized characterization (particle size, polymorphism, thermal analysis).
Why is GMP compliance important for analytical services?+
GMP-compliant analytical data is required for regulatory submissions and batch release. Non-GMP data cannot be used for these purposes. GMP compliance means: validated analytical methods, qualified and calibrated instruments, trained and qualified analysts, complete documentation (audit trail, data integrity), sample management and chain of custody, and regular audits by regulatory authorities or clients.
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