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  • (040) 6744 8888
Techsol Life Sciences
Techsol Life Sciences
 
 
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  • CAPABILITIES
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  • Safety management During early Phase Clinical Trials
    Leveraging Pre-Clinical Data to Optimize Patient Safety Management During Early Phase Clinical Trials
    July 10, 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
  • Clinical Trial eSource Implementation
    Enabling eSource in Clinical Studies to Optimize Trial Quality
    November 17, 2021
  • eConsent for Clinical Trials
    Implementing Electronic Consent for Clinical Trial Participation
    October 19, 2021
  • Clinical Trial Site Selection
    Data Driven Site Selection for Clinical Trials in a Post-COVID-19 World
    September 20, 2021
  • Clinical Trial Site Selection
    4 Effective Strategies to Accelerate Site Selection to Activation
    September 14, 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
  • Techsol Life Sciences Private Limited, CRO Services Division, #845, Road No: 45, Ayyappa Society, Madhapur, Hyderabad, Telangana 500081
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Featured Solutions

  • Medical Writing
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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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