ANALYTICAL DEVELOPMENT

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TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract Manufacturing ANALYTICAL DEVELOPMENT • Monitoring of the first industrial manufacturing batches. • Characterization of raw materials according to Pharmacopoeia. • Development and validation of analytical techniques. • Quantification of active ingredients, impurities and degradation products in raw materials and medicines. • Transfer of analytical techniques. • In vitro dissolution profiles. TECNALIA´s Pharmaceutical Development Laboratory is accredited by the Spanish Medicines Agency (AEMPS) in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). We offer solutions in several dosage forms formulation: • Solids (tablets, capsules, sachets, etc.) • Liquids (suspensions, solutions, syrups, etc.). • Semi-solids (gels, creams, ointments, etc.).

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Biopharmaceutical ProductsContract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)Analytical MethodsAnalytical DevelopmentDrug Formulation (general category)Pharmaceutical Machinery & TechnologyProductsServices

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Biopharmaceutical ProductsContract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)Pharmaceutical Machinery & Technology

TecnaliaTECNALIA Pharma Labs is a full-service Contract Development, Manufacturing Organization (CDMO) that provides high quality services under a strong quality system, with over two decades serving the pharmaceutical industry. We provide comprehensive services across the entire value chain (human medicines, medical devices, & veterinary medicines). • Pharmaceutical development: Galenic & Analytical Development, Stability Studies • Manufacturing: Contract Manufacturing of Industrial Batches

ANALYTICAL DEVELOPMENT

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