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New drugs and clinical trials rules 2019: Changes in responsibilities of the ethics committee

Neelu Singh, NiveditaJ Madkaikar, ParthaM Gokhale, DevenV Parmar

2020Perspectives in Clinical Research38 citationsDOIOpen Access PDF

Abstract

March 2019 by Government of India. New rules have set specific requirements for ethics committee (EC). The EC is required to follow requirements set as per New rules and to forward their report to Central Licensing Authority (CLA). This document is divided into different sections like definitions and applicable chapter & schedules for EC; changes related to registration of clinical studies and biomedical and health research; changes related to constitution, functions, proceedings, responsibility of EC for clinical trial; maintenance of records by EC; suspension and cancellation of registration of EC, post-trial access of drugs, changes and clarity related to academic clinical trials and role of ECs in compensation and medical management process.

Topics & Concepts

Clinical trialCLARITYEthics committeeSet (abstract data type)Government (linguistics)Research ethicsMedicineProcess (computing)Political scienceMedical educationPublic administrationComputer sciencePathologyPsychiatryBiologyPhilosophyBiochemistryOperating systemProgramming languageLinguisticsBiomedical Ethics and RegulationEthics in Clinical ResearchHealth Systems, Economic Evaluations, Quality of Life
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