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Publication:
Current perspective of severe adverse events and compensation requirements in India

dc.contributor.affiliationDepartment of Clinical Operations, SIARAM Clinical Research Centre, Bikaner, Rajasthan, India
dc.contributor.affiliationDepartment of Oncology, Acharya Tulsi Regional Cancer Treatment and Research Institute, Sardar Patel Medical College and AG of Hospitals, Bikaner, Rajasthan, India
dc.contributor.authorGoyal, Shekhar
dc.contributor.authorKapoor, Akhil
dc.contributor.authorBhadu, Indra
dc.date.accessioned2026-10-11T17:56:02Z
dc.date.issued2014-08-01
dc.description.abstractAs per Drug Controller General of India (DCGI), there are clear cut compensation guidelines for clinical trial participants in case of death and injury after amendment in schedule Y (Rule 122DAB - Compensation in case of injury or death during clinical trial). The purpose of these guidelines is to provide Severe Adverse Event (SAE) compensation calculation as well as determination of the ratio of amount in clinical trial injury.
dc.identifier.citationInt J Clin Trials. 2014;1(2):76-77.
dc.identifier.doihttps://doi.org/10.5455/2349-3259.ijct20140809
dc.identifier.issn2349-3259
dc.identifier.issn2349-3240
dc.identifier.otherojs:ijct:47
dc.identifier.urihttps://mediparchive.org/handle/123456789/44
dc.language.isoen
dc.publisherMedip Academy
dc.relation.ispartofInternational Journal of Clinical Trials
dc.rightsCopyright (c) 2015 International Journal of Clinical Trials
dc.source.urihttps://www.ijclinicaltrials.com/index.php/ijct/article/view/47
dc.subjectAdverse events
dc.subjectClinical trial
dc.titleCurrent perspective of severe adverse events and compensation requirements in India
dc.typeArticle
dc.typeLetter to the Editor
dspace.entity.typePublication
journal.titleInternational Journal of Clinical Trials
oaire.citation.endPage77
oaire.citation.issue2
oaire.citation.startPage76
oaire.citation.titleInternational Journal of Clinical Trials
oaire.citation.volume1

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