Public Faq | National Medical Research Register

General NMRR FAQ

How does NMRR guide its users ?

NMRR is designed to be an intuitive system where all applicants can learn to use with the aid of comprehensive on-line guidance, supported by the Helpdesk and other published sources of advice on applications. A public user guideline is also available in the NMRR website.

NMRR 2.0 works better in which browser?

It works well in all the browers. Preferred browser: Mozila Firefox , Chrome and Egde

What are the documents that I need to prepare before registering my study in NMRR?

For registration of a study in NMRR , the documents required are curriculum vitea (CV) of all the study team members (investigators) , GCP certificate (mandatory for all study team in interventional study) and Investigator's Agreement - Head of Department (HOD's) - Institutional Agreement (IA-HOD-IA) form. All documents together with information background of the intended study need to be listed and uploaded in NMRR.

What is IA-HOD-IA and COI form?

Investigator's Agreement - Head of Department (HOD's) - Institutional Agreement (IA-HOD-IA) form is a document required during registration and submission to scientific review and ethical approval while Declaration of Conflict of Interest (COI) form is only required during the submission to scientific review and ethical approval . Both of these prefilled documents will be generated while filling up the research details during registration process. Investigator is required to complete the (IA-HOD-IA) form ( to be completed individually by Principal Investigator (PI) , PI at site and at least 1 sub-investigator (for each study site without PI at site)) and Declaration of Conflict of Interest (COI) form (to be completed by PI) and reupload the complete form whenever necessary during the submission process.

Does the reseacher need to pay any processing fee?

As for now, there is no processing charges or fee implemented for any of the submission and registration in NMRR