Please visit ijn.com.my for the detailed listing of patient visiting hours.
Are children allowed to visit patients at IJN?
Children under 12 years of age are allowed to visit from 6:00 pm to 8:00 pm only and are not permitted in the units or at the waiting areas of the Intensive Care Unit (ICU) and Coronary Care Unit.
Why do I need to have a Visitor Pass?
We require everyone entering the Hospital to identify themselves and their destination to provide a safer environment for our patients, visitors and staff. Visitors are advised to get the visitor’s pass at the Information Counter (located in the main lobby),15 minutes prior to the official visiting hour.
How can I contact a patient in the Intensive Care Unit?
Intensive Care Unit patients have no phones in their rooms. Intensive Care Unit nurses will relay information to immediate family members only.
Do you have a listing of hotels in the InstitutJantung Negara area?
Yes, we have Putra Hotel in front of IJN. For a more detailed listing, please visit ijn.com.my
How do I get to IJN?
IJN is located at the heart of Kuala Lumpur on JalanTunRazak. You may use public transportation such as taxi directly to IJN or the LRT with the stop at the Titiwangsa LRT station before taking the taxi to IJN.
If you are coming from the Kuala Lumpur International Airport (KLIA) via taxi, the journey to IJN will take approximately 40 minutes
As a participant in a clinical trial, you have the right:
To have enough time to decide whether or not to participate and to make that decision without any pressure from the people who are doing the research.
To address any questions you have to the research team and or Principal Investigator at any time.
To refuse to participate in the study/clinical trial, and to stop participating at any time after you begin the study.
Your decision will not affect your right to your usual care not related to the research.
To be informed why the study/clinical trial is being done, what will happen, and what you will be asked to do if you are in the study.
To be informed about any reasonably foreseeable risks, discomforts or side effects that may occur during participation.
To be informed whether there are any costs associated with being in the study and whether you will receive any reimbursement for participating in the study.
To be informed who will have access to information collected about you, and how your confidentiality will be protected.
To be informed whom to contact directly with questions about the research, about research-related injury, and about your rights as a research subject.