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  • Princeton Office
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  • 101 College Road East Princeton NJ 08540 USA
  • info@techsollifesciences.com
  • Kothaguda, Kondapur, Hyderabad, Telangana 500084
  • (040) 6744 8888
Techsol Life Sciences
Techsol Life Sciences
 
 
  • CLINICAL
    • Clinical Development Services
      • Scientific And Medical Writing
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      • Drug Safety And Pharmacovigilance
      • Regulatory Lifecycle Management
      • Launch & Commercialization
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      • Medical Monitoring & Review
    • Clinical Study Expertise
      • Therapeutic Areas
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      • Observational Studies
      • Investigator Initiated Studies
      • Real World Evidence
      • Post-Marketing Clinical Follow-Up
      • Registry Trials
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      • Food & Nutraceuticals
    • Clinical Technology Services
      • AccelClinical
      • Oracle Clinical One
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      • CTMS & Site Payments
      • Electronic Trial Master File
      • Clinical Oversight Platform
  • REGULATORY
    • Regulatory Affairs
      • Regulatory Strategy & Due Diligence
      • Regulatory Intelligence (RI)
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      • Regulatory Agency Liaison
      • GMP Compliance Services
      • Regulatory Lifecycle Management
      • CMC Regulatory Affairs Consulting
    • Regulatory Operations
      • CMC Regulatory Documentation Authoring
      • Regulatory Submissions & Applications
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    • Regulatory Consulting
  • PHARMACOVIGILANCE
    • PV Consulting & Functional Services
      • Drug Safety Case Processing
      • Aggregate Safety Reports
      • Literature Monitoring
      • Safety Signal Management
      • QPPV & LPPV Services
      • PSMF Lifecycle Management
      • Medical Device Vigilance
      • PV Risk Management
      • Medical Information Call Center
      • PV Audits & Training Services
      • PV Regulatory Intelligence
    • Safety Technology Services
      • Oracle Argus Safety Services
      • Empirica Signal Management
      • E-Submission Gateways
      • Argus Safety Service Desk
      • Safety Data Analytics
      • Safety Database Migration Services
    • PV Ops Management Platform
      • Compier Regulatory Intake
      • Compier ICSR Management
      • Compier Agreements & Reconciliation
      • Compier Aggregate Reports
      • Compier Literature Screening
      • Compier PSMF
      • Compier PV Ops Oversight
  • QUALITY & LABS
    • Quality Management System
      • TrackWise Implementation & Validation
      • TrackWise System Integrations
      • TrackWise EQMS Application Support
      • Quality Insights Generation
    • Biopharma Research & Development
      • IDBS E-Workbook
      • IDBS Polar
    • Quality & Labs Image
  • MEDTECH
    • Medical Writing & Clinical Affairs
      • Clinical Affairs Strategy
      • Medical Device Registration
      • MedTech Medical Writing
      • Clinical Investigation & Evaluation
      • Technical Files & Dossier Preparation
      • 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
      • Validation & Assurance Services
      • System Integration Services
      • Data Science & Artificial Intelligence
      • 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
      • AccelSafety
      • AccelCTMS
      • Compier PV Ops
      • SciMax Medical Information
      • SciMax Publications
      • SCIMAX Collaboration Portal
      • SCIMAX IIT Portal
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      • SCIMAX Grants Portal
  • ABOUT
    • About US
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      • Company Overview
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      • Meet Our Team
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      • Contact Us
    • Resource Library
      • Case Studies
      • Insights
      • Events
      • White Papers
      • Press Releases
  • Understanding the Importance of CMC (Chemistry, Manufacturing, and Controls) documents in the Pharmaceutical Product Lifecycle
    April 8, 2024
  • MoCRA Cosmetics Regulatory Compliance FDA Techsol Life Sciences
    MoCRA Made Easy: A Comprehensive Guide to Cosmetic Safety Compliance
    January 29, 2024
  • Oncology R&D Pipeline and De-Risk Clinical Trials
    Understanding how Disease Registries can Power Oncology R&D Pipeline and De-Risk Clinical Trials
    January 24, 2024
  • 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
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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

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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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