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Techsol Life Sciences
Techsol Life Sciences
 
 
  • CLINICAL
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  • REGULATORY
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    • Specialized & Niche Services
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  • PHARMACOVIGILANCE
    • PV Capabilities Overview
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      • Integrated & Automated Functional Services
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      • Oracle Argus Safety One Cloud
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      • Axway E-Submission Gateway
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    • PV Oversight & Agentic AI
      • Compier PV Ops & Agentic AI
      • Intake – Inbox & Correspondence
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    • PV Functional Services
      • TOTALVigilance Services
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      • Safety Signal Management
      • QPPV & LPPV Services
      • PSMF Lifecycle Management
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      • Med Info Contact Center
      • Materiovigilance Services
      • PV Audits & Training Services
      • PV Regulatory Intelligence Services
  • QUALITY & LABS
    • Quality Management System
      • TrackWise Implementation & Validation
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  • MEDTECH
    • Medical Writing & Clinical Affairs
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      • Device Approval Submissions Support
    • Device Vigilance & Reporting
      • Safety Data Management
      • Medical Device Reporting (MDR)
      • Post-marketing Surveillance Support
      • PSUR Submissions
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      • EU PMS – FSCA Reporting
    • Regulatory Affairs & Labeling
      • Regulatory Lifecycle Management
      • EU MDR / IVDR Consulting
      • Product Certification: CE Marking
      • Medical Device Labeling
      • Post-Market & Regulatory Support
      • Medical Device Artwork Management
  • CAPABILITIES
    • Pharma Digital Transformation
      • Strategic Technology Consulting
      • Validation & Assurance Services
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      • Intelligent Process Automation
      • Custom Applications Development
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      • Teaming Partner Services
    • Clinical And Data Services
      • Early Phase Clinical Trials
      • Phase II – III Clinical Research
      • Phase IV & Real-World Evidence
      • Medical Device Solutions
    • Technology Platforms
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      • Compier PV Ops
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  • ABOUT
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    • Resource Library
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      • Insights
      • Events
      • Press Releases
  • CASE STUDY ON REGULATORY STRATEGY DEVELOPMENT AND DOSSIER SUBMISSION SUPPORT
    June 10, 2025
  • CASE STUDY ON MEDICAL DEVICE PRODUCT REGISTRATION IN INDIA
    June 10, 2025
  • CASE STUDY ON STRUCTURED PRODUCT LABELING (SPL)MANAGEMENT SERVICES
    June 9, 2025
  • Case Study on Clinical Evaluation of Prosthodontic products
    May 27, 2025
  • Implementation and Validation of a Cloud-based Clinical Data Management System
    Implementation and Validation of a Cloud-based Clinical Data Management System for a Leading Pharmaceutical Company
    January 24, 2024
  • Axis Clinicals | Techsol Life Sciences
    Implementation and Validation of Phase 1 Clinic Automation System for Axis Clinicals
    December 29, 2022
  • Hugel Logo | Techsol Life Sciences
    Argus Safety Cloud Implementation and Validation on Oracle Cloud for HUGEL Pharma
    December 29, 2022
  • IPCA
    Establishing an Integrated Global Drug Safety and Signal Management Cloud Solution
    December 29, 2022
  • Gemvax & KAEL | Techsol Life Sciences
    Argus Safety Cloud Implementation on Oracle Cloud for KAEL-GemVax
    December 27, 2022
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  • Uncategorized
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Techsol Life Sciences
  • Techsol Life Sciences, 101 College Road East, Princeton, New Jersey, 08540, USA
  • Techsol Life Sciences Private Limited, Plot No: 845, Road No: 45, SBH Officers Colony, Mega Hills, Ayyappa Society, Madhapur, Hyderabad, Telangana 500081
  • 040-45038660

Featured Solutions

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  • Compier
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  • AccelCTMS
  • AccelStudy

Recent Posts

  • Understanding the Importance of CMC (Chemistry, Manufacturing, and Controls) documents in the Pharmaceutical Product Lifecycle April 8, 2024
  • MoCRA Made Easy: A Comprehensive Guide to Cosmetic Safety Compliance January 29, 2024
  • Understanding how Disease Registries can Power Oncology R&D Pipeline and De-Risk Clinical Trials January 24, 2024
  • Mastering Medical Device Registrations: A Guide to Navigating Regulatory Pathways July 12, 2023

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