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Techsol Life Sciences
Techsol Life Sciences
 
 
  • CLINICAL
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  • REGULATORY
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  • PHARMACOVIGILANCE
    • PV Consulting & Functional Services
      • Drug Safety Case Processing
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      • Compier Regulatory Intake
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      • Compier Aggregate Reports
      • Compier Literature Screening
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      • Compier PV Ops Oversight
  • QUALITY & LABS
    • Quality Management System
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  • MEDTECH
    • Medical Writing & Clinical Affairs
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    • Device Vigilance & Reporting
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      • Post-marketing Surveillance Support
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      • Literature Search and Review
      • EU PMS – FSCA Reporting
    • Regulatory Affairs & Labeling
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      • EU MDR / IVDR Consulting
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      • Medical Device Labeling
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  • CAPABILITIES
    • Pharma Digital Transformation
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      • Phase II – III Clinical Research
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      • Compier PV Ops
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  • ABOUT
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    • Resource Library
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  • PV Signal Management
    Best Practices for Signal Management in Pharmacovigilance
    December 3, 2021
  • Compier Aggregate Reporting
    Aggregate Reporting – Significance, Classification and Challenges
    September 2, 2021
  • Literature screening
    Literature Screening – Process overview, challenges en-route and the scope for automation
    August 30, 2021
  • eTMF Evolution
    How the Trial Master File is Expected to Evolve in the Next Three Years
    July 28, 2021
  • Pharmacovigilance Automation
    Automation Opportunities in Pharmacovigilance
    June 25, 2021
  • Outsourcing PV Process
    Factors Influencing the Outsourcing of Pharmacovigilance Processes
    January 13, 2021
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
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Featured Solutions

  • Medical Writing
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  • Pharmacovigilance
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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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