28
Oct
2025
Conscio Group
Exhibitor at CPHI Frankfurt 2025 stand 5.1F1, Contract Manufacturing and Services
About Us
Categories
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DE
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2015On CPHI since
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3Certificates
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250 - 499Employees
Company types
Primary activities
Event information
CPHI Frankfurt 2025
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28 Oct 2025 - 30 Oct 2025
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Messe, Frankfurt
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Visit us at stand 5.1F1, Contract Manufacturing and Services
Products Featured at CPHI Frankfurt 2025
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Product Innovation & Formulation
Innovation & Formulation: We offer pharmaceutical R&D, feasibility studies, proof-of-concept, formulation development and analytical method development for multiple dosage forms such as solids, semi-solids, liquids, oral films, and transdermal patches. We can work with over 30 pharma technologies f... -
Product Clinical solutions: Trials
Conscio's in-house clinical Unit has been operating since 2007, with more than 600 BA/BE/PK studies completed and proprietary of over 270 validated bioanalytical methods. Equipped with a 60-bed on-site clinical unit in Prague and a recently opened 36-bed unit in Ostrava, we provide comprehensive services w... -
Product Clinical Solutions: Bioanalysis of small and large molecules
We provide a wide range of GCP/GLP bioanalytical services for preclinical and clinical studies with human and/or veterinary drug products up to Phase III. We offer development and validation of bioanalytical methods in different biological matrices; complete bioequivalence studies; pharmacokinetics/toxicok... -
Product Quality control: Pharmaceuticals
Conscio offers GMP-certified and ICH-compliant chemistry, manufacturing and controls assays (CMC) as well as analytical support during validation of manufacturing processes. Samples are analyzed by approved and validated methods for routine batch testing, stability studies, analyses of high potency product... -
Product Quality Control: Biopharmaceuticals
Conscio is among the few CROs with both GLP and GMP services for large molecules, peptide & protein IMPs or biosimilars. Our services include method transfer and validation, bioanalysis and ADA immunogenicity with ELISA, ECLA, UPLC or LC-FTMS, as well as GMP quality control, characterizations, capillar... -
Product Manufacturing Solutions
We are GMP-certified for the manufacturing of IMP clinical batches (Phases I-III) as well as commercialized products. Our laboratories are prepared to work with over 30 key pharmaceutical technologies, all API types from OEB classes 1-5 and narcotics, innovative technologies, hard-to-make formulations in a...
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