Compare CDMOs with analytical method development and validation expertise. Filter by analytical technique, molecule type, and regulatory filing support.
592 companies listed
Analytical method development creates the test procedures used to measure drug product quality attributes (potency, purity, impurities, dissolution, etc.). Method validation demonstrates that these procedures are suitable for their intended purpose per ICH Q2 (R2) guidelines. Together, they form the analytical foundation for every pharmaceutical product.
CDMOs offering method development and validation services support the entire product lifecycle: from early development (screening methods, forced degradation) through clinical manufacturing (validated methods for batch release) to commercial production (transfer, trending, lifecycle management). Strong analytical CDMOs reduce development timelines by executing method work in parallel with formulation and process development.
Thailand
Biolab Company Limited is a leading Thai pharmaceutical manufacturer with 45+ years of experience, producing pharmaceuticals, dietary supplements, and cosmeceuticals. The company operates a 24,000 sqm factory in Samut Prakan, Thailand with OEM/ODM contract manufacturing capabilities. Certified PIC/S GMP (Singapore HSA), EU GMP, ISO/IEC 17025, Halal, and Thai FDA Quality Award. Exports to 20+ countries.
India
Biological E Limited is an Indian biopharmaceutical company focused on vaccine development and manufacturing, with production capacity of up to 1 billion vaccines annually. They offer contract manufacturing for vaccines and biologics, with FDA-registered facilities performing analysis, API manufacture, labeling, manufacturing, and packing. Partners include Bavarian Nordic for chikungunya vaccine manufacturing.
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