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Cato Research
Cato Research is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them.
Company Contact:
Christine Federovitch
Phone:919.361.2286
Fax:919.361.2290
Email:icfederov@cato.com
Website:http://www.cato.com
Address:Westpark Corporate Center 4364 South Alston Avenue Durham, NC 27713-2280
Christine FederovitchPhone:
919.361.2286Fax:
919.361.2290Email:
icfederov@cato.comWebsite:
http://www.cato.comAddress:
Westpark Corporate Center 4364 South Alston Avenue Durham, NC 27713-2280 - South Africa
- Switzerland
- Romania
- Israel
- India
- Germany
- Europe
- Croatia
- Austria
- Asia
- Africa
- USA
CLINICAL DEVELOPMENT
Clinical Services Provided
Clinical TrainingData/IT/StatisticsBiostatisticsData ManagementInformaticsMedical Monitoring/SafetyMedical WritingPost-MarketingProject ManagementProtocol DevelopmentRegulatory/Quality/SafetyElectronic sbmissionsPharmacovigilanceQuality AssuranceRegulatoryRisk AssesmentsSafety/PharmacovigilanceSite/Study/InvestigatorInvestigator RecruitmentSite AuditSite ManagementSite SelectionStudy MonitoringStudy Supply Management
Formulations Administered
Also active in fields: pharmacovigilance
CONSULTANT
Areas of Expertise
BD/HR/IT/LegalBusiness developmentCompany and product valuationsDue DiligenceProduct launch Strategic consultingFacilities/EquipmentContractor Selection/ManagementEquipment and process validationPackagingResearch/DevelopmentAnalyticalAPIAuditsClinicalCMCDiscovery ResearchFormulationPharmacokineticsPharmacologyProduct DevelopmentProgram/Project ReviewProject managementQuality AssuranceQuality ControlRegulatorySOPsToxicology
Formulation Categories-Consultant
FORMULATION/MANUFACTURING
Development Stage
REGULATORY
Formulation Category
Also active in fields: pharmacovigilance, (eCTD) Electronic Common Technical Document , Clinical Trial Exemptions (CTXs), Division of Drug Marketing, Advertising, and Communications (DDMAC), Drug Master File Annual (DMF), Marketing Authorization Applications (MAAs), Orphan Drug Applications (ODAs), Premarket Approvals (PMAs)
