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Nuvisan Pharma Services
The NUVISAN Group is a successful, globally active and independent Clinical Research Organization (CRO), which conducts clinical research Phases I through III with a special focus on Oncology. Well over 2,500 pharmaceutical studies have been conducted since the company was founded. Along with complementary divisions focusing on bioanalytics, biopharmaceuticals, pharmaceutical analysis, stability testing and clinical trial supply production and packaging, the Nuvisan Group is able to offer comprehensive services in all areas of clinical pharmaceutical development from a single source. Founded in 1979 and headquartered in Neu-Ulm, Germany, the approx. 450 highly qualified employees of the NUVISAN Group around the world provide the pharmaceutical industry with the experience and expertise needed in todays competitive environment. In addition to NUVISAN GmbH, other companies belonging to the NUVISAN Group include FOCUS Clinical Drug Development GmbH and Essex Pharma Development GmbH. NUVISAN has been a member of the ADCURAM Group AG since May 11, 2010.
Company Contact:
Lonnie Barish
Phone:
+1 925-803-1080
Fax:
+49 731 9840–280
Email:
Lonnie.Barish@nuvisan.com
Website:
http://nuvisan.com
Address:
Corp: Wegenerstrasse 13, 89231 Neu-Ulm, Germany
Lonnie BarishPhone:
+1 925-803-1080Fax:
+49 731 9840–280Email:
Lonnie.Barish@nuvisan.com Website:
http://nuvisan.comAddress:
Corp: Wegenerstrasse 13, 89231 Neu-Ulm, Germany- Russia
- Germany
- France
- Europe
- Serbia
- Spain
ANALYTICAL
API Type
Sample Type
Service Type
MethodsMethod DevelopmentMethod TransferMethod ValidationTests - Dissolution/DisintegrationDisintegrationDissolution App. I/IIDissolution App. IIIDissolution App. IVTests - Impurities/DegradationForced DegradationImp./Deg QuantitationTests - PhysicalParticle SizePhysical TestingTests - Protein/Peptide/DNA/OligoPeptide mappingProtein Carbohydrate AnalysisProtein Chemical StabilityTests - StabilityICH/Commercial Stability StorageICH/Commercial Stability TestingPhotostabilityStability Storage (I/II)Stability Testing (I/II)Tests/Analysis - OtherAssay/PotencyExtractables/LeachablesLCMS AnalysisMetals AnalysisMoistureRadiolabel AnalysisResidual Ethylene OxideResidual Solvent AnalysisTets - ReleaseLot and Batch Release TestingTransdermal Patch Characterization
BIO-ANALYTICAL
CLINICAL DEVELOPMENT
Clinical Services Provided
Data/IT/StatisticsBiostatisticsData ManagementPost-MarketingProject ManagementProtocol DevelopmentRegulatory/Quality/SafetyQualified Person ReleaseQuality AssuranceRegulatorySafety/PharmacovigilanceSite/Study/InvestigatorInvestigator EducationPatient Recruitment/RetentionSite AuditSite ManagementSite SelectionStudy MonitoringStudy Supply Management
Clinical Study Type
Formulations Administered
CONSULTANT
Areas of Expertise
FACILITY REGULATORY STATUS
Facility regulatory bodies
Facility subcategories
FORMULATION/MANUFACTURING
API/Business Sector Types
Development Stage
Formulation Type
PACKAGING/FILLING/LABELING
Development Stage
Packaging Filling Services
Child-ResistantClinical Package/LabelCold Chain ManagementControlled Substance PackagingFilling ServicesBottlesInserts/OutsertsLabel design and printingPackaging Identification and SourcingPackaging SuppliesPackaging ValidationPrimary Package FillingPrivate Label PackagingSecondary PackagingTamper Proof Closures
PREFORMULATION
REGULATORY
Formulation Category
Regulatory Services
SUPPLY CHAIN MANAGEMENT

