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  • (040) 6744 8888
Techsol Life Sciences
Techsol Life Sciences
 
 
  • CLINICAL
    • Clinical Development Services
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      • AccelClinical
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  • REGULATORY
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  • PHARMACOVIGILANCE
    • PV Consulting & Functional Services
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      • Medical Information Call Center
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    • Safety Technology Services
      • Oracle Argus Safety Services
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    • PV Ops Management Platform
      • Compier Regulatory Intake
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      • Compier Literature Screening
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      • Compier PV Ops Oversight
  • QUALITY & LABS
    • Quality Management System
      • TrackWise Implementation & Validation
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      • Quality Insights Generation
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  • MEDTECH
    • Medical Writing & Clinical Affairs
      • Clinical Affairs Strategy
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      • Clinical Investigation & Evaluation
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      • Device Approval Submissions Support
    • Device Vigilance & Reporting
      • Safety Data Management
      • Medical Device Reporting (MDR)
      • Post-marketing Surveillance Support
      • PSUR Submissions
      • Literature Search and Review
      • 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
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      • System Integration Services
      • Analytics & Insights Generation
      • Intelligent Process Automation
      • Custom Applications Development
      • Data Standards Consulting
      • 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
      • SciMax Medical Information
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  • ABOUT
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      • Press Releases
  • Medical Device Registrations | Techsol Life Sciences
    Mastering Medical Device Registrations: A Guide to Navigating Regulatory Pathways
    July 12, 2023
  • Safety management During early Phase Clinical Trials
    Leveraging Pre-Clinical Data to Optimize Patient Safety Management During Early Phase Clinical Trials
    July 10, 2023
  • Lay Summary for Clinical Trials - Techsol Life Sciences
    Authoring Accurate and Concise Lay Summary for Clinical Trials to comply with EU CTR Requirements
    April 27, 2023
  • Techsol EU MDR Medical Device Labelling Services
    Navigating Through EU MDR and IVDR Medical Device Labelling Requirements
    April 24, 2023
  • Clinical Trial Design Simulation - Techsol Life Sciences
    Clinical Trial Design Simulation Through Data Powered Statistical Computing
    March 24, 2023
  • AI in Clinical Trials | Techsol Life Sciences
    Practical Applications, Benefits and Risks of Using Artificial Intelligence in Clinical Trials Subjects Screening
    February 27, 2023
  • Clinical Trial Protocol Deviations Violations
    How to Proactively Prevent Clinical Trial Protocol Deviations and Protocol Violations
    July 4, 2022
  • Food & Nutra Clinical Trials
    Food & Nutraceuticals: How Companies can Prove Health Value with Clinical Trials
    December 20, 2021
  • PV Signal Management
    Best Practices for Signal Management in Pharmacovigilance
    December 3, 2021
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Categories
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Techsol Life Sciences
  • Techsol Life Sciences, 101 College Road East, Princeton, New Jersey, 08540, USA
  • Techsol Life Sciences Private Limited, Technology Services Division, Level – 4, Lorven Tiara, Survey No.34, Kondapur, Hyderabad, Telangana 500084
  • Techsol Life Sciences Private Limited, CRO Services Division, #845, Road No: 45, Ayyappa Society, Madhapur, Hyderabad, Telangana 500081
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Recent Posts

  • Mastering Medical Device Registrations: A Guide to Navigating Regulatory Pathways July 12, 2023
  • Leveraging Pre-Clinical Data to Optimize Patient Safety Management During Early Phase Clinical Trials July 10, 2023
  • Authoring Accurate and Concise Lay Summary for Clinical Trials to comply with EU CTR Requirements April 27, 2023
  • Navigating Through EU MDR and IVDR Medical Device Labelling Requirements April 24, 2023

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