Global Manufacturer Pages

PRA International

(732) 578-5400

4 Industrial Way W.
Eatontown, New Jersey, USA   07724

http://www.prainternational.com

pra is one of the world's leading global clinical development organizations with more than 3,000 employees worldwide delivering reliable service, program-level therapeutic expertise, easy global access to knowledge and an involved senior management to our customers.

Products & Services

    • Global
    • Contract Research Organization
    • Cro
    • Clinical
    • Development
    • Organization
    • Clinical Development Organization
    • Clinical Trial
    • Clinical Trials
    • Trial
    • Trials
    • Management
    • Development Trials
    • Design
    • Consulting
    • Services
    • Consulting Services
    • Allergy
    • Respiratory
    • Product Development
    • Product
    • Development
    • Cardiovascular
    • Cns
    • Oncology
    • Therapeutic
    • Protocol Design
    • Protocol
    • Case Report Form
    • Crf
    • Patient Recruitment
    • Patient
    • Feasibility
    • Data
    • Informed Consent Form
    • Icfs
    • Pharmacology
    • Phase I
    • Phase Ii
    • Phase Iii
    • Phase Iv
    • Phase I-iv
    • Postmarketing Surveillance
    • Postmarketing
    • Surveillance
    • Biostatistics
    • Biostatistical Analysis Reporting
    • Biostatistical
    • Analysis
    • Reporting
    • Pharmacokinetics
    • Pharmacodynamics
    • Regulatory Consulting
    • Regulatory
    • Pharmaceutical
    • Biotechnology
    • Medical
    • Device
    • Principal Investigator
    • Investigator
    • Investigators
    • Investigational
    • New Drug
    • Drug
    • Applications
    • Ind
    • Ndas
    • Investigate
    • Electronic Data Capture
    • Edc
    • Regulatory
    • Fda
    • Mca
    • Ctx
    • Submissions
    • Approval
    • Support Services
    • Clinical Research Associate
    • Cras
    • Cra
    • Careers
    • Clinical Research
    • Clinical
    • Research
    • Medical Monitoring
    • Monitoring
    • Data Safety
    • Safety
    • Monitoring Boards
    • Monitoring
    • Dsmbs
    • Dsmb
    • Institutional Review Board
    • Irbs
    • Irb
    • Data Monitoring Committee
    • Dmcs
    • Dmc
    • Electronic Regulatory Submission
    • Pivotal
    • First Time In Man
    • Studies
    • Gcp Auditor
    • Gcp
    • Auditor

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