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Development Center for Biotechnology
The Development Center for Biotechnology (DCB) of Taiwan is a nonprofit organization founded in 1984. Co-sponsored by government grants and private donations, DCB's purpose is to advance Taiwan's biotech-pharma industry by building infrastructure, developing key technologies, and training talented workforces in coordination with government, industry, and academic institutions.
Company Contact:Wei-Kuang Chi
Phone:+886-2-2695-6933
Fax:+886-2-2695-7597
Email:weikchi@mail.dcb.org.tw
Website:http://www.dcb.org.tw
Address:101, Lane 169, Kangning St., Xizhi Dist, New Taipei City 22180, Taiwan, R.O.C.
  • Taiwan
ANALYTICAL
API Type
BiologicalSmall Molecule
Sample Type
APIDosage form
Service Type
Differential Scanning CalorimetryMethodsMethod DevelopmentMethod TransferMethod ValidationTests - Impurities/DegradationForced DegradationImp./Deg QuantitationTests - Protein/Peptide/DNA/OligoDNA TestingElectrophoresisElisa/Western BlotProtein Aggregation/DeaggregationProtein Biophysical CharacterizationProtein Carbohydrate AnalysisProtein Chemical StabilityProtein Dosage FormProtein Primary StructureProtein Secondary/Tertiary StructureTests - StabilityAccelerated StabilityICH/Commercial Stability StorageICH/Commercial Stability TestingStability Storage (I/II)Stability Testing (I/II)Tests/Analysis - OtherAssay/PotencyFourier Transform Infrared Analysis LCMS AnalysisTets - ReleaseLot and Batch Release Testing
API/BIOLOGICS/REAGENTS
API Development Stage
DiscoveryGMP clinicalPreclinical
API Services
Biosimilar ManufactureCell Bank ManufacturingFermentationProcess Dev.PurificationScale-up
API Types
BiologicsAntibodyProtein
Reagents
PEG Reagents
BIO-ANALYTICAL
Services
Assays and SuppliesBioassaysCell CultureProtein BindingDiscovery SupportDrug-Drug InteractionsElisa/Western BlotGeneralMethods Development and ValidationMicrobiologyGMP-GLPBioanalytical GLPBioanalytical GMPPre-GLPMetabolite IdentificationPCR
DISCOVERY/PRECLINICAL
Discovery Services
Cell AssaysChemistryMedicinal ChemistryLeads/TargetsLead Optimization
Therapeutic Areas
Antiinflammatory/ImmuneBiologicsCancerEndocrine/MetabolismInfectious DiseasesWound Care
FACILITY REGULATORY STATUS
Facility regulatory bodies
EUFDA
Facility subcategories
Qualified/accredited
FORMULATION/MANUFACTURING
API/Business Sector Types
AntibioticBiologicalSmall Molecule
Development Stage
FormulationFormulation DevelopmentGLP/Tox SupportManufacturingGMP Clinical (Phase I/II)Scale upProcess Development
Formulation Type
InhalationInjectableOral
PHARMACOKINETICS
Service Types ADME
ADME- In vitroADME/PK-In vivoCaCo-2DMPK
PREFORMULATION
Preformulation Services
Accelerated StabilityParticle size measurements Physical PropertiesPkaSolubility
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