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Clinical Research

af Niti Mittal
Clinical Research af Niti Mittal
Bag om Clinical Research

· Comprehensive content covering all aspects of clinical research. · Evolving paradigms in clinical research, e.g. modelling and simulation, artificial intelligence, etc. · Milestones in the evolution of drug regulations in India · Drug regulatory framework in India and key ICH countries. · Evolution of drug pricing mechanisms and IPRs in India. · Updated text incorporating the New Drugs and Clinical Trials Rules 2019; Guidelines on BA/BE studies; ICMR National Ethical Guidelines 2017; National Guidelines for Stem Cell Research 2017; Medical Devices Rules 2017. · Latest amendments and guidelines on ethics committees, informed consent, electronic informed consent, compensation and ICMR Policy on Research Integrity and Publication Ethics 2019. · Templates for various documents like patient information sheet, assent document, case report form, adverse event reporting form etc.

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  • Sprog:
  • Engelsk
  • ISBN:
  • 9789389974447
  • Indbinding:
  • Hardback
  • Sideantal:
  • 508
  • Udgivet:
  • 1. april 2023
  • Størrelse:
  • 196x32x241 mm.
  • Vægt:
  • 1135 g.
  • 2-3 uger.
  • 11. december 2024
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Beskrivelse af Clinical Research

· Comprehensive content covering all aspects of clinical research.
· Evolving paradigms in clinical research, e.g. modelling and simulation, artificial intelligence, etc.
· Milestones in the evolution of drug regulations in India
· Drug regulatory framework in India and key ICH countries.
· Evolution of drug pricing mechanisms and IPRs in India.
· Updated text incorporating the New Drugs and Clinical Trials Rules 2019; Guidelines on BA/BE studies; ICMR National Ethical Guidelines 2017; National Guidelines for Stem Cell Research 2017; Medical Devices Rules 2017.
· Latest amendments and guidelines on ethics committees, informed consent, electronic informed consent, compensation and ICMR Policy on Research Integrity and Publication Ethics 2019.
· Templates for various documents like patient information sheet, assent document, case report form, adverse event reporting form etc.

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