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Tech Observer
Tech Observer is a a quality-driven Global Clinical Research Organization (CRO) providing full-service analytical support across the entire product development cycle. Our specialized domains include Clinical Monitoring, Clinical Data Management, Statistical/SAS Analyses, Scientific Communication, Pharmacovigilance and Regulatory Affairs. We pride ourselves on our ability to provide innovative quality solutions to meet clinical challenges, all delivered RIGHT ON TIME.EVERY TIME. Our industry-standard, validated SAS and data management system, compliant with ICH GCP guidelines and 21 CFR Part 11 regulations is a guarantee that you will always be provided with data of the highest quality. Additionally, keeping in mind that every clinical need is different, we offer our clients the flexibility to customize a plan based on our various offerings, choosing a few or several of our service options.
Company Contact:
Priyanka Sachdev
Phone:
+91-11-28524382
Email:
BusDev@tech-observer.com
Website:
http://cro.tech-observer.com
Address:
375 Main Street Suite# 201 Hackensack, NJ 07601
Priyanka SachdevPhone:
+91-11-28524382Email:
BusDev@tech-observer.comWebsite:
http://cro.tech-observer.comAddress:
375 Main Street Suite# 201 Hackensack, NJ 07601- USA
- United Kingdom
- Japan
- India
- France
CLINICAL DEVELOPMENT
Clinical Services Provided
Clinical TrainingData/IT/StatisticsBiostatisticsClinical Trial SimulationsData ManagementInformaticsEpidemiology/Health OutcomesInstitutional Review Board (IRB)Medical Monitoring/SafetyMedical WritingPost-MarketingProject ManagementProtocol DevelopmentRegulatory/Quality/SafetyElectronic sbmissionsPharmacovigilanceQuality AssuranceRegistries/Observational StudiesRegulatoryRisk AssesmentsSafety/PharmacovigilanceSite/Study/InvestigatorInvestigator EducationInvestigator RecruitmentOnsite Pharmacy/CompoundingPatient Recruitment/RetentionSite AuditSite ManagementSite SelectionStudy MonitoringStudy Supply Management
Clinical Study Type
Bioavailability/BioequivalenceBiomarkersPharmacogenomicsPharmacology/PathologyClinical PathologyClinical PharmacologyPhase 1 to 2Dose RangingFirst-in-Human StudiesPhase IPhase IIPhase IIaPhase 3Phase 4PK/PDSafety/TolerabilitySpecialized StudiesAge/GenderDrug Alcohol InteractionsDrug Drug InteractionsFood EffectGenotypingMicro dosingQT EvaluationSkin sensitization and irritation studiesSpecial PopulationsTaste/Sensory Evaluation
Formulations Administered
Therapeutic Area
Anesthesia/PainCancerCardiovascularCNSCritical CareEndocrine/MetabolismGastrointestinalGenitourinaryHematologyInfectious DiseasesInflammation/ImmuneMedical DevicesMens HealthMusculoskeletal DiseasesOphthalmologicalOrthopaedicsOsteologyPediatricsPlasma ProductsRespiratorySkin DiseasesVaccinesWomens HealthWound Care
CONSULTANT
DISCOVERY/PRECLINICAL
REGULATORY

