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    clinical research center​

    Zenovel, your trusted partner for Regulatory Compliance and Clinical Research Quality Assurance

    GCP

    • Audit
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    • Sponsor Oversight
    • QMS Set up
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    • CRO Setup & upgradation
    • CSV
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    Zenovel, your trusted partner for Regulatory Compliance and Clinical Research Quality Assurance

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    Drug Dev. & Discovery

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    Pre-Clinical

    Zenovel, your trusted partner for Regulatory Compliance and Clinical Research Quality Assurance

    Services Overview
    GCP
    • Audit
    • Risk Based Monitoring
    • Pre-Inspection Readiness
    • Sponsor Oversight
    • QMS Set up
    • Project Management
    • PK-Stat Review
    • CRO Setup & upgradation
    • CSV
    • Training
    • Contract Staffing
    GMP
    • Audit
    • Consulting
    • Plant Setup/Upgradation
    • Pre-Inspection Readiness
    • Global Audit Library
    • QMS Set up
    • CSV
    RA Services
    • Pre-submission services
    • Regulatory Intelligence Services
    • AI-powered Regulatory Affairs Services
    • Regulatory Consulting
    • Due Diligence of Dossier
    • Dossier Templates
    • Local Regulatory partner for EU/US
    • Batch release & batch testing site support
    • Biologics Registration Services
    • Regulatory Compliance and GAP Analysis
    • Local QP support for batch release in EU
    • Local QPPV support
    • Dossiers In Licensing and Out Licensing
    • eCTD compilation
    • CO/NCO
    • User Testing Services
    • Lifecycle Management (LCM)
    • Regulatory Staffing Services
    • Bibliographic Application
    • Post Submission Services
    Drug Dev. & Discovery
    • Chemistry Services
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  • India
  • 906,907, Silver Radiance 4, Sarkhej - Gandhinagar Hwy, Sola, Ahmedabad, Gujarat 382481, India
  • +91-635-635-3636
  • Australia
  • 9, Blaxland Avenue,
    Cranbourne North,
    Victoria-3977, Australia
  • Brazil 
  • Rua Praia do Tubarão, Quadra C,Loteamento Eco Vilas, Lote 13 – Vilas do Atlântico 42708-730 Lauro de Freitas, Bahia, Brazil
  • Brazil 
  • R. Álvaro Müler, 932 - Vila Angelino Rossi, Campinas-SP,13023-240, Sao Paulo, Brazil.
  • USA
  • 911 Hwy 6 Hitchcock,
    Texas, 77563, USA
  • Canada
  • 215 Moorlands Crescent,
    Kitchener, Ontario N2P 0C3
  • China
  • Zhenjiang Tech Park, Shanghai China
Copyright © 2024 Zenovel. All rights reserved.
Zenovel
  • Discover Zenovel
    • About Zenovel
    • History
    • Founder
    • Worldwide Reach
    • Milestone
    • Experience
  • Services
    • GCP
      • Audit
      • Risk Based Monitoring
      • Pre-inspection Readiness
      • Sponsor Oversight
      • QMS Setup
      • Project Management
      • Pk Stat Review
      • CRO Setup & upgradation
      • CSV
      • Training
      • Contract Staffing
    • GMP
      • Audit
      • Consulting
      • Plant Setup & Upgradation
      • Pre-Inspection Readiness
      • Global Audit Library
      • QMS Set up
      • CSV
    • RA Services
      • AI-powered Regulatory Affairs
      • Regulatory Intelligence Services
      • Regulatory Compliance and GAP Analysis
      • Due Diligence of Dossier
      • Pre-submission services
      • CO/NCO
      • Dossier Templates (USA & EU)
      • Dossiers In Licensing
      • Dossiers Out Licensing
      • Bibliographic Application
      • eCTD compilation
      • Biologics Registration Services
      • Local Regulatory partner for EU/US
      • Lifecycle Management (LCM)
      • Post Submission Services
      • Batch release & batch testing site support
      • Local QP support for batch release in EU
      • User Testing Services
      • Local QPPV support (UK PL ES NL DE HR etc)
      • Regulatory Staffing Services
    • Drug Dev. & Discovery
      • Chemistry services
      • Biology services
      • Formulation and analytical services
    • Key Expert Services
      • IT-enabled services
      • Pre-clinical Support
      • Intellectual Property Services
      • Medical & Scientific Writing
      • Strategic and Business services
      • CMC Development
  • Competency
    • GCP
    • GMP
    • Regulatory Affairs
  • Resources
    • Blog
    • FAQ
    • Case Studies
    • Guideline Summaries
    • White Papers
Partner with us
Submit RFP