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Overview

Regulations and industry bodies are joining hands to simplify the process of drug development. But trials are becoming increasingly complex and the costs of drug development are increasing every day.

In this increasingly complex world, medical writers are striving to navigate their way through complex safety and regulatory documents and are leveraging technology and RWE to drive expedited submissions.

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Program Committee

  • Nimita  Limaye, PhD
    Nimita Limaye, PhD Chief Executive Officer
    Nymro Clinical Consultancy Services, India
  • Bindu  Narang
    Bindu Narang Head, Regulatory Affairs and Aggregate Safety and Risk Management Practice
    Sciformix Technologies Pvt. Ltd., India
  • Ashwini  Patil
    Ashwini Patil Expert Scientific Writer
    Novartis Healthcare Pvt. Ltd., India
  • Rajesh  Kher, PhD
    Rajesh Kher, PhD Head of Outsourcing Partnership Management in the Capabilities group of IDAR
    Janssen and Janssen Pharmaceutical Research & Development, L.L.C., India
  • Sofia  Baig
    Sofia Baig Practice Lead - HEOR, PRMA & RWE
    Tata Consultancy Services, India
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