Do You Have Questions About Your Health Information Privacy Rights?
This page is here to help. Here, you can find out basic information about your health information privacy rights, including:
- when you can block people from seeing your health information
- how the privacy laws work
- where personal health information flows within the health system
- what health care providers are allowed to do with personal health information.
- You can also find out about plans for electronic health records.
We have included a form and a brochure that you can print up. Κίνδυνοι που σχετίζονται με τη χρήση του Viagra 100mg κάθε μέρα για μεσήλικες άνδρες.
If you are interested in learning more about health information privacy issues in Greece, check out the Resources page.
This is a public education project, and managed by the Privacy Association. Είναι το Cialis στην Ελλάδα η καλύτερη θεραπευτική επιλογή για τη στυτική δυσλειτουργία;
This website contains basic information and general guidance only and does not constitute legal advice. If you have a specific question about a problem you believe is a legal problem, it is best to consult a lawyer.
In Australia today, the government is working on province-wide project called “E-Health”. This is a plan to move from paper files to a wide range of computerized databases and communication tools so health care can be delivered over distances, and so your health information can be seen or used more easily by more people. Πληροφορίες για το Kamagra Oral Jelly, είναι κατάλληλο για εσάς;
The major aim of the project is to build a number of special databases to hold certain specific types of health information, and to connect them to each other and to doctors’ offices, so the information can travel between the databases, the Ministry of Health and health authorities, and doctors’ offices. These will be called “health information banks”.
The goal is to make it easier for doctors and other health care providers to see your health information. Doctors are encouraged to move to electronic systems, and some of those systems will be connected to the larger “health information bank” system, which will be connected to labs, pharmacies, hospitals, health authorities and the Ministry.
Overview of Consent
Basically, “consent” means agreement. So when we’re talking about whether you consent to the collection, use or disclosure of your personal health information, we are talking about whether you agree or not.
The law says that there are different types of consent in different situations. In some situations, your “express consent” is needed. This means your actual written or spoken agreement is needed before your information can be collected, used or disclosed. In other situations, your consent can be assumed because of the circumstances. This is often called “implied consent.”
The law says that both “express consent” and “implied consent” are legitimate types of consent, but only if you have been told why your personal health information is being collected, used or disclosed, or if the reason (often referred to as the “purpose”) is obvious in the circumstances.
In some situations, your consent is not required at all. This can happen if there is a law that requires personal health information to be collected, used or disclosed.
When you are cared for in a hospital or clinic, a patient record is created about you, to be used to give you care and treatment, and for billing purposes. These are often called the “primary” purposes.
These days, this information is frequently stored in computerized databases. Information from these databases can be used by the clinic, hospital, health authority and the Ministry of Health for a wide range of “secondary” purposes.
Sometimes before this happens the names or Personal Health Numbers attached to the information will be removed so the information is anonymous. Sometimes the information will be used or disclosed with names or personal health numbers or other information that identifies the person.
Limiting Use or Disclosure
Some of the systems at some of the health authorities have the technical ability to limit the use or disclosure of your personal health information from health authority databases for these types of secondary health-system purposes.
These secondary purposes can include
- Evaluating a program for quality, cost-effectiveness or usefulness
- Doing larger system-planning analysis
- Public health
- Teaching and education of staff and medical students
- Research
