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How can I promote my published research?
Share your publication on social media, present your findings at conferences, and include it in your CV. It is a great satisfaction to see your research getting published and acknowledged by the global scientific community.
Share your publication on social media, present your findings at conferences, and include it in your CV. It is a great satisfaction to see your research getting published and acknowledged by the global scientific community.
See lessWhat are the potential benefits of publishing in a peer-reviewed journal for my career?
It demonstrates your research expertise, enhances your academic reputation, and can be crucial for securing future research funding or employment opportunities.
It demonstrates your research expertise, enhances your academic reputation, and can be crucial for securing future research funding or employment opportunities.
See lessWho reviews my ethical approval application?
KAHER’s research ethics committee consisting of experts from various disciplines. They will review your application and decide whether to approve, request revisions, or reject your proposal.
KAHER’s research ethics committee consisting of experts from various disciplines. They will review your application and decide whether to approve, request revisions, or reject your proposal.
See lessIs KAHER’s ethics committee registered and accredited?
KAHER boasts as one of the very few ethics committees in India who have received NABH accreditation for ethics committee as well as SIDCER-FERCAP recognition (International). The ethics committee is registered with CDSCO and DHR for regulatory and academic clinical trials, respectively.
KAHER boasts as one of the very few ethics committees in India who have received NABH accreditation for ethics committee as well as SIDCER-FERCAP recognition (International). The ethics committee is registered with CDSCO and DHR for regulatory and academic clinical trials, respectively.
See lessWhat happens if my application is rejected?
If your application is rejected, the ethics committee will provide feedback on the areas needing improvement. You must address these concerns and resubmit your application.
If your application is rejected, the ethics committee will provide feedback on the areas needing improvement. You must address these concerns and resubmit your application.
See lessHow long does the ethical approval process typically take?
The review process usually takes several weeks to a few months. Best will be to contact the IEC Secretariat who will be able to guide you better.
The review process usually takes several weeks to a few months. Best will be to contact the IEC Secretariat who will be able to guide you better.
See lessDo I need to seek approval for any changes to my research design after initial approval?
Yes, if you make any changes to your research design, you must inform the ethics committee and seek approval for any amendments. Only administrative changes are allowed. You must consult your Supervisor/Guide and IEC Secretariat to ensure this.
Yes, if you make any changes to your research design, you must inform the ethics committee and seek approval for any amendments. Only administrative changes are allowed. You must consult your Supervisor/Guide and IEC Secretariat to ensure this.
See lessWhat are my responsibilities regarding reporting adverse events?
If any unexpected or harmful events occur during your research, you must report them immediately to the ethics committee within 24 hours.
If any unexpected or harmful events occur during your research, you must report them immediately to the ethics committee within 24 hours.
See lessWhat is CTRI?
: CTRI is the Clinical Trials Registry - India (CTRI) launched on 20th July 2007 is managed by the ICMR-National Institute of Medical Statistics, New Delhi, India. The CTRI ( www.ctri.nic.in) is an online, free and searchable system for the prospective registration of all clinical studies being condRead more
: CTRI is the Clinical Trials Registry – India (CTRI) launched on 20th July 2007 is managed by the ICMR-National Institute of Medical Statistics, New Delhi, India. The CTRI ( http://www.ctri.nic.in) is an online, free and searchable system for the prospective registration of all clinical studies being conducted in India. In addition, the CTRI also registers clinical studies being conducted in countries which do not have a Primary Registry of their own.
See lessWho is responsible for registering a trial?
A responsible Registrant, Trialist or User is authorized to register clinical trials in the CTRI. Registration in the CTRI is needed to gain access to this facility. The "Registrant" for a trial is either the principal investigator (PI) or the primary sponsor, to be decided by an agreement between tRead more
A responsible Registrant, Trialist or User is authorized to register clinical trials in the CTRI. Registration in the CTRI is needed to gain access to this facility. The “Registrant” for a trial is either the principal investigator (PI) or the primary sponsor, to be decided by an agreement between the parties. The primary sponsor is ultimately accountable for ensuring that the trial is properly registered. For multi-center and multi-sponsor trials, it is the lead PI or lead sponsor who should take responsibility for registration.
See less