Princeton Office
  • Princeton Office
  • Hyderabad Office
  • 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
      • Clinical Operations & Study Monitoring
      • Clinical Data Management
      • Biostatistics & SAS Programming
      • Regulatory Affairs
      • Drug Safety And Pharmacovigilance
      • Regulatory Lifecycle Management
      • Launch & Commercialization
      • Data Safety Monitoring Board
      • Medical Monitoring & Review
    • Clinical Study Expertise
      • Therapeutic Areas
      • Early Phase Studies
      • Observational Studies
      • Investigator Initiated Studies
      • Real World Evidence
      • Post-Marketing Clinical Follow-Up
      • Registry Trials
      • Patient Surveys
      • Food & Nutraceuticals
    • Clinical Technology Services
      • AccelClinical
      • Oracle Clinical One
      • AccelStudy
      • EPRO & ECOA
      • CTMS & Site Payments
      • Electronic Trial Master File
      • Clinical Oversight Platform
  • REGULATORY
    • Regulatory Affairs
      • Regulatory Strategy & Due Diligence
      • Regulatory Intelligence (RI)
      • Health Authorities Interactions
      • Regulatory Agency Liaison
      • GMP Compliance Services
      • Regulatory Lifecycle Management
      • CMC Regulatory Affairs Consulting
    • Regulatory Operations
      • CMC Regulatory Documentation Authoring
      • Regulatory Submissions & Applications
      • e-CTD Preparation & Submissions
      • DMF Compilation & Submission
      • Product Registration & Import License
      • Regulatory Information Management
      • Regulatory QMS & Audit Support
    • 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
      • SCIMAX EAP Portal
      • SCIMAX Grants Portal
  • ABOUT
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  • Cloud Assistance
    FDA’s proposed guidance on CSA
    May 25, 2021
Categories
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  • CTMS
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  • Validation & Assurance
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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

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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