Forms and Guidelines

​​Submission Forms

Forms Listed below are the research forms required for your Research proposal submission. Contact the MRC Research Administrator 00974 439-2440 if you have questions or need forms not provided here.

The forms are available in MS Word format. Click on the icon for display or download to your PC. 

Download All the Forms Required for your Research Proposal Submission


File ​Name
 ​
Description
File Type
Download
Research Proposal Submission Form
To be used for all Retrospective or Prospective studies submitting to MRC
Doc
Case Report Submission Form
To be used for all case reports or case series submitting to MRC
Doc
Ethical Extension Request Form
To be used for all Research proposals for renewing the time frame for the ethical approval.
Doc
Progress Report Form​
To be submitted bi-annualy
Doc
Research project Completion Report Form
Dr. Kholode Al Hail
Doc
Adverse Event Form
To be used for submitting the final results of the study
Doc
Guidelines for Lab Animal Use
Please read the guidelines for Lab Animal Use. 
Doc
IACUC Approval
To be used for IACUC Proposal application form for use of animals in research. 
Doc​


Consent Forms:


File ​Name 
Description
File Type
Download​
Generic Signed Informed Consent Form
To be used for all prospective researches which involve more than minimal risk to patients; and involves identification of participants. Thiis consent documents the research participants agreement to take part in research activities, by signing the consent document.
Doc
Waiver of Signed Informed Consent Form​
To be used in prospective researches which present no more than minimal risk of harm to participants and where signed informed consent is not required under normal circumstances. Examples are: Implied consent, verbal consent, oral consent, telephonic consent etc..
Doc
Genetic Consent Form- A
To be used in genetic research where the samples collected are identifiable and there is an intervention by the investigators to reveal the results of the genetic tests to the research participants, families, or their health care providers.
Doc
Genetic Consent Form- B
To be used in genetic research where the samples collected are identifiable but there is no intention to disclose results of the genetic tests to research participants, families or their health.
Doc
Genetic Consent Form- C
To be used for these genetic researchers with truly unidentifiable samples (no codes or indirect identifiers) but there is a possibility of risk to research participants should in advertantt disclosure occur.
Doc
Genetic Consent Form- D​
To be used for these genetic researches using truly unidentifiable samples (with no codes or indirect identifiers) and the risk to research participants is low, in case inadvertant disclosure occurs.
Doc
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